The Library

Welcome to the Library, where you'll find a selection of industry resources including eBooks, Whitepapers, Webinars, Survey Reports, Research Reports and more.

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LIBRARY

The Basics of Biotech 101, 201 & 301

Webinar | Price: Individual Session: $129 | Full Series: $299

This 3-part webinar series is specifically geared toward the non-science professional who needs to better understand industry terminology, science, techniques and issues. This series provides an overview of the science and technology used to enable discovery and the processes scientists use to discover new therapeutics. Download now.

2015 L.E.K. Strategic Hospital Priorities Study: Hitting an Inflection Point for Hospital Suppliers and MedTechs

Whitepaper | Sponsored by: L.E.K. Consulting

The MedTech industry has hit an inflection point and opportunities abound for companies to deliver broader solutions that healthcare providers are looking for. L.E.K. Consulting presents a hospital segmentation framework that illustrates four dimensions of changes affecting providers and defines six main areas of strategic focus to drive success for MedTechs. Download White Paper Today.

Medical Writing and Technical Writing: Why you Need an Expert

Whitepaper | Sponsored by: Watermark Research Partners

Medical and Technical writing is a complex challenge for pharmaceutical, biomedical, and medical device companies. A professional experienced medical and technical writing team can perform the tasks including the research, in a shorter period of time. Find out how we can help.

Mitigating Risk and Speeding Development with Advanced Capsule Technology

Webinar | Wednesday, June 3rd | 11am ET / 8am PT | Presented by: Capsugel

This webinar will explore capsules' utility in a range of applications, including bioavailability enhancement, modified release, pediatric solutions, & fixed dose combinations. Learn more about how capsules enable rapid advancement of products built on QbD principles and supported by PAT. Register today!

Supply Network Visibility for Emerging Biotechs

Webinar | Thursday, June 4th | 1pm ET / 10am PT | Presented by: Collaborative Consulting

This webinar is the first in a series that explores insights and approaches to attaining drug supply integrity while addressing the challenges of disconnected, opaque supply networks and Drug Supply Chain Security Act (DSCSA) regulatory compliance. Reserve Your Spot Today!

Virtualizing High Performance Computing To Advance Science Research - A Roundtable Discussion

Webinar | Wednesday, June 10th | 2pm ET / 11am PT | Sponsored by: EMC

While virtualization is widely used in commercial enterprise environments, it has not to date played any significant role in High Performance Computing (HPC). During this webinar we discuss the promises and challenges in this new, emerging area. Reserve Your Spot Today!

Using ePRO with Smart Devices: A Case Study

Webinar | Wednesday, June 10th | 1pm ET / 10am PT | Presented by: Rho

Interest in using electronic patient reported outcomes (ePRO) on smart devices is on the rise. In this webinar, Emily Cantrell and Becky Baggett will share lessons learned working on a large phase 3 pain study that utilizes ePRO on tablet devices. Register Now!

Virus Safety of Biopharmaceuticals: Risk Mitigation during Upstream and Downstream Operations

Webinar | Thursday, June 11th | 1pm ET / 10am PT | Sponsored by: Catalent

This webinar will review regulatory guidance and practical strategies for designing viral clearance studies. These include appropriate scale-down of unit operations, virus spike-related considerations and validation (clearance evaluation) of manufacturing process steps. Reserve Your Spot Today!

Survey | The Paperless TMF: An Industry Benchmark

Whitepaper | SPONSORED BY: Veeva Systems

This research survey will examine industry attitudes toward electronic master files (eTMFs). How are eTMFs holding up against trial documents on paper? As a thank you for your time and input, the first 50 respondents will receive a $5 Amazon eCard. Complete the Survey Today!

How to enable anywhere, any data access without compromising security

Webinar | Tuesday, June 16th, 1pm ET/10am PT | SPONSORED BY: M-Files

This webinar will discus how the emergence of the ability to share documents and data across thousands of miles instantly has pulled biopharma companies in two opposing directions. Companies want, even need, the interconnectivity that is facilitated by the Internet, but feel equally strongly about controlling who can view and interact with their data. Register Today!

Adherence-Informed Clinical Trials to Achieve and Maintain Maximal Treatment Efficacy

Webinar | Tuesday, June 23 | 11:00am ET / 8:00am PT | Presented By: MWV Healthcare

This webinar will address the impact of medication non-adherence in clinical trials. Accurate adherence measurement is necessary to evaluate a compound's true potential and increase the likelihood of a successful trial outcome. Register today!

mHealth + Patient Engagement: A new connected health model

Webinar | NOW AVAILABLE ON-DEMAND | Presented By: BBK Worldwide

BBK Worldwide hosts a webinar exploring this new connected health model and its impact on clinical research. Join their expert panel, which includes mHealth experts from BBK Worldwide, Oracle and Empatica, and learn key strategies for successful implementation. Registration is free – click here.

Proactive Planning: How Supply Chain Risk Mapping Can Prevent Costly Disruptions

Webinar | Wednesday, July 22nd | 11am ET / 8am PT | Sponsored by: UPS

Biopharma companies can never eliminate the risk of supply chain disruption, but they can prevent some problems and prepare themselves for others. Knowing every company in the supply chain--from tier one down--and having contingency plans in place are essential steps to foreseeing and responding to disruptions. Maps of supply chain risks give companies this knowledge. Register Now!

Delivering on the Vision of a Truly Integrated Customer Engagement Platform

Webinar | NOW AVAILABLE ON-DEMAND | Presented by: Pegasystems and Telerx

Join Pegasystems and Telerx to learn how the Pega platform is being utilized to support a multi-tenant client environment to engage patients during all phases of a product's life cycle, through a central touchpoint. Register to Watch Now!

Maximizing the Value of Real World Evidence – How Life Sciences Organizations Can Benefit from Health Analytics

Webinar | Tuesday, June 30th | 2pm ET / 11am PT | Sponsored by: SAS

This webinar will bring together pharmaceutical executives and data-analytics experts to explain the basics of using data in health settings, the technology available for sifting through real-world data, and effective strategies for putting the data to work for the company. Reserve Your Spot Today!

A No-Nonsense Discussion About Life Science Data-Intensive Computing With SPARK

Webinar | Now Available On-Demand | Sponsored by: EMC

Scientific workflows like light-sheet microscopy and next generation sequencing are pushing research groups to develop new methods to deal with such data-intensive instrumentation. Current, mostly serialized analysis pipelines can often take days to run and often there is no 'right analysis'. Reserve today to watch now!

Bringing a Small Molecule to Clinic: A Guide for Start-Up Development Programs

eBook | Published: May 26, 2015 | Sponsored by: Catalent

It's time to transition your molecule discovery to a commercial drug launch. This guide is your roadmap for arriving at your desired destination quickly and without making costly mistakes along the way. Download now.

Survey | 2015 Life Sciences Promotional Content Management Survey

Survey | Published: May 22nd, 2015 | Sponsored by: Veeva Systems

This research survey will examine industry attitudes toward pharmaceutical and biotech promotional content management process and systems. Are there areas for efficiency improvement? As a thank you for your time and input, the first 50 qualified respondents will receive a $5 Starbucks eCard. Complete the Survey Today!

Lessons-learned from Executing Complex Medical Device Trials - Special focus on Cardiovascular Device

Webinar | NOW AVAILABLE ON-DEMAND | Presented by: Medpace

Medpace uses its vast experience in CV trials as a backdrop to discuss the critical factors for designing and executing studies for complex and high-risk medical devices. Register to Watch Now!

Expanding The Face Of Meta-Data in Next Generation Sequencing - A Roundtable Discussion

Webinar | Now Available On-Demand | Sponsored by: EMC

Join this webinar to take part of the discussion evolving nature of metadata along with recent advancements and approaches developed by the IRODS Consortium and its members to capture, manage, and use meta-data to enable life science research workflows. Reserve today to watch now!

Worried about Your Next FDA Meeting? Key Tips to Make It a Success

Webinar | NOW AVAILABLE ON-DEMAND | Presented by: Rho

Regulatory authority meetings require strategic preparation to ensure a successful outcome. In this webinar, Lauren Neighbours, Clinical Research Scientist, and Dana Minnick, Regulatory Scientist, discuss how to approach FDA meetings to get the most benefit for your development program. Register to Watch Now!

Ending Stagnation: How Collaboration Tools are Enabling a New Era of R&D

eBook | Published: May 6, 2015 | Presented By: Polycom

Biopharma R&D, from drug discovery through to late-phase clinical trials, suffers from two fundamental, near industry-threatening problems: It is too slow and too expensive. Something has to change. Fortunately for the industry, tools and tactics that can shave time and money from drug development already exist. Download this eBook to learn more.

Is Service a Cost? Or Revenue Stream?

Whitepaper | Sponsored by: Watermark Research Partners

The long term success of any product depends on lifecycle performance. SteelHorse Medical offers a national technical services team that can perform field or factory repair, technical support, and all other Technical Service functions. Learn more and download today.

Biosimilars: Getting Cheaper Biologics to the Market

eBook | Published: May 4, 2015 | Sponsored by: Catalent

On March 6, 2015, 5 years after the Biologics Price Competition and Innovation Act of 2009 was signed into law, the FDA finally approved a biosimilar drug. Although the approval capped the FDA's years-long process to establish a pathway for biosimilars, experts question whether much has actually changed for the prospects of getting biosimilars to market in the U.S. Download this eBook to learn more.

2015 Life Science Industry Trends – Focus on Measuring Training Effectiveness

Whitepaper | Published On: May 1, 2015 | Presented By: UL EduNeering

Advance beyond basic qualifications and identify skill gaps throughout the training process by utilizing learning tools that measure both technical and competency skills. Download the whitepaper today!

Key Scientific Considerations and Concepts in Developing a Global Observational Study Protocol

Webinar | NOW AVAILABLE ON DEMAND | Sponsored by: Parexel

This webinar will summarize the core scientific concepts needed to develop a global observational study protocol that describes or evaluates a therapeutic treatment in patients under conditions of usual care, in terms of clinical, humanistic and economic outcomes for a variety of key stakeholders. Register to watch now!

Managing Federally Funded Biotechnology Projects: Keys to Successful Execution

Webinar | Sponsored by: Lexem Strategy | NOW AVAILABLE ON-DEMAND

This webinar will demonstrate how government contracts differ in the marketplace. Business cases from the HHS - Biomedical Advanced Research and Development Authority and the DOD will provide a thorough understanding to navigate this landscape of management, legality, contracts, and oversight. Reserve Your Spot Today!

How to Build a TMF Strategy to be Inspection-ready

Webinar | Thursday, April 16th | 2pm ET / 11am PT | Sponsored by: Veeva Systems

Hear how Kythera Biopharmaceuticals reduced their TMF reconciliation time by 40% with their TMF strategy. Sign up for the webinar here.

The TMF Reference Model: It Doesn't Have to be Scary

Webinar | NOW AVAILABLE ON-DEMAND | Presented by: Rho

At first glance, the TMF reference model seems daunting, especially for smaller companies. In this webinar, Kristen Snipes and Missy Lavinder share tips and tricks for making the process manageable based on their own recent experience implementing the model. Register to Watch Now!

Leveraging Cloud to Enable Agility in Regulated Environments

Webinar | Now Available On Demand | Presented by: Veeva

Learn how Natera leverages cloud-based content management systems to simplify collection, management, and secure access of controlled documents - improving operational efficiency, and enabling agility amidst increasing procedural requirements. Register to watch now!

Biopharma's Balancing Act: Information Access vs. Security and Compliance

eBook | Published: March 30, 2015 | Sponsored by: M-Files

Over the past few years a series of events have crystallized fears about data security into solid intel on real and significant threats against biopharma businesses. And yet, with biopharma globalizing and disaggregating, companies cannot afford to shut off from the world. This is the dilemma faced by biopharma CIOs in 2015. Download today!

What Do Customers Need in Oral Dose Development

eBook | Published: March 30, 2015 | Sponsored by: Catalent

Oral dose development is the goal of many drug developers. The translation of a drug-design concept to the delivered oral dose can be complicated, and understanding the needs of drug company clients, as well as patients and doctors, is a vital part of the process. Download this eBook to learn more.

Powering Product Development in Skin Care with Metabolic Profiling

Webinar | NOW AVAILABLE ON-DEMAND | Presented by: Metabolon

Here we describe discovery approaches designed to broadly survey the skin metabolome as well as focused metabolomic assessment of sebum, stratum corneum, skin biopsy, cell culture and reconstructed skin models across a variety of conditions. Further, we share results from recent publications and practical clinical case studies. Register to Watch Now!

Understanding the New FDA Guidance on Data Standards

Webinar | NOW AVAILABLE ON-DEMAND | Presented by: Rho

In December 2014, FDA released the Guidance for Industry "Providing Regulatory Submissions in Electronic Format—Standardized Study Data." This webinar will review the guidance and discuss the implications for Sponsors currently conducting studies and for those starting new studies soon. Register to Watch Now!

Next Generation of Functional Outsourcing Models

Webinar | NOW AVAILABLE ON DEMAND | Presented By: Parexel

This webinar will discuss the evolution of Functional Outsourcing Models from insourcing to functional strategic partnership. Register today!

New Technologies for Complex Oral Formulation and Drug Delivery Challenges

eBook | Published: January 16, 2015 | Sponsored by: Catalent

As the knowledge of the basic biology behind disease increases, and as drugs become more advanced, delivery challenges increase for oral and other formulations. Because of this, delivery solutions need to become more sophisticated and more effective. Download this eBook to learn more.

Targeting cancer treatments: A progress report

eBook | Sponsored by: Catalent | Published: December 16, 2014

Throughout the history of cancer drug development, researchers have tried to make treatments more specific, reducing the side effects and increasing the efficacy. The next step in this process is the move towards therapies that are not only tailored to each individual, but that also target tumors and nothing else. Download this FierceBiotech eBook to learn more.

Analyzing Real-World Data for Lifecycle Management

eBook | Published: October 27, 2014 | Sponsored by: Covance

Life used to be simpler for pharma commercialization teams. Once a drug won regulatory approval, the path to sales was relatively clear. Now a drug must prove to payers its value over existing treatments and continue to do so throughout its lifecycle. Download this FierceBiotech Special Report to learn more.

Special Report | The Changing Landscape of Phase IV Research

eBook | Published: September 29, 2014 | Sponsored by: Covance

Industry spending on post-authorization studies belies the rapid changes occurring in Phase IV research, driven by an the demand for evidence of safety and effectiveness. Download this Special Report to learn how Phase IV research continues to transform.

Animal Health Leaders Embrace Biotech R&D

eBook | Published: September 15, 2014 | Sponsored by: Catalent

The presence of biotechs in the animal health industry is growing. Companies working in this industry are using biologic processes to develop large-molecule drugs and vaccines for both livestock and pets, and to improve techniques for research, development, and manufacturing. Download this eBook to learn more about the role biotechs play in the burgeoning animal health industry.

Cross-Contamination in Drug Manufacturing: The Regulatory Trends

eBook | Published: July 25, 2014 | Presented by: One 2 One

Cross-contamination among production lines is an important issue in drug manufacturing, because it can put both patients and workers at risk of adverse health effects. As the global therapeutics markets grow and drugs become increasingly more potent, authorities in the U.S., Europe and elsewhere are tightening regulations to increase safety and control exposure. Download this eBook to learn more.

Optimizing Formulation Development: New HPMC Capsules Offer Expanded Options for Pharmaceutical Formulations

eBook | Published: July 18, 2014 | Presented by: Capsugel

The evolution of technology in pharmaceutical and medical sciences has extended the range of polymers that are being developed to meet the demand for quality in capsule manufacturing. While they were initially targeted to the producers of vitamins and minerals, these plant-based capsules are now becoming an important option for pharmaceutical manufacturers. Download this eBook to learn more today!

Executive Summary | Veeva 2014 Paperless TMF Survey: An Industry Benchmark

eBook | Published: July 7, 2014 | Sponsored by: Veeva

FierceMarkets and Veeva Systems recently conducted a survey of more than 250 Trial Master File (TMF) owners to explore the impact of growing eTMF adoption as well as the drivers, benefits, and barriers to going paperless. The survey examines the success factors for fully electronic trials and gives an industry-wide view of where organizations fall on the spectrum of paper-based to paperless TMFs. Download this free Executive Summary today!

Next-Generation Orphan Drug Delivery

eBook | Published: May 19, 2014 | Sponsored by: Catalent

According to the National Organization for Rare Disorders (NORD), a disease is rare if it affects fewer than 200,000 Americans. There have been around 6,800 rare diseases defined so far, affecting around 30 million people in the US alone. Big Pharma used to ignore this segment of the market, but now developing orphan drugs to treat these rare diseases is an industry priority. Download this eBook today!

eBrief | Work Smarter: How Data and Informatics are Reshaping Post-Approval for Pharma

eBook | Published: May 5, 2014 | Sponsored by: Enclarity, a LexisNexis company

With all of pharma’s key markets rethinking reimbursement, the onus is on companies to find ways to deliver the evidence payers want. The rise of new sources of real-world data and the informatics capabilities to derive insights from the figures gives pharma a way to meet these demands. But to make the most of the information, the industry must re-think its practices. Download this eBrief today!

The Future of Animal Health

eBook | Published: March 17, 2014 | Sponsored by: Catalent

The current market for animal drugs and vaccines (not just dogs and cats) is worth $22 billion a year and growing. Add in the huge and growing market for livestock treatments and it's no surprise pharmaceutical companies are angling to find the ideal position in animal health. This FiercePharma eBook will survey the landscape in animal health and the potential growth opportunities for investors and life sciences entrepreneurs. Download this eBook today!

eBrief: Securing Clinical Documents in Cloud-Based Collaborations

eBook | Published: February 18, 2014 | Sponsored by: NextDocs

Big pharma and biotech companies have undergone a series of consolidations, as internal research budgets continue to shrink. With much more at stake, the industry is evolving to embrace more collaborative, future-thinking tools that will not only save sponsors money, but that will also increase efficiency, expedite trials and help identify ineffective drugs sooner. Download this eBrief today!

Renal Biomarkers: Driving Drug and Diagnostic Development in Kidney Disease

eBook | Sponsored by: MPI Research | Published: November 22, 2013

Biomarkers have been used in the diagnosis and monitoring of kidney disease for many years. However, these are most effective in established disease, and by the time they detect injury, the damage may already be done. This ebook discusses the use of biomarkers in identifying susceptibility to kidney disease, using biomarkers to predict outcomes, as well as the limitations of existing biomarkers. Learn more.

New Drugs For Old: Failed Drugs Gaining a Second Chance

eBook | Sponsored by: Catalent | Published: November 18, 2013

The cost of drugs that fail in clinical trials can be measured by far more than the cash poured into the development process. Now, through drug repositioning some of those investment costs can be recouped by giving drugs a second and often lower-risk chance in a new indication. Download this FierceBiotech ebook to learn key advantages and strategies of drug repositioning.

Picking Winners: Data Mining for Drug Discovery

eBook | Sponsored by: Certara | Published: November 4, 2013

There are several new initiatives being undertaken in the biopharmaceutical industry aimed at making better use of the vast terabytes of information flowing out of research labs around the world. This ebook discusses the intelligent application of analytics and informatics to enable drug hunters to better understand disease, pharmacological and clinical data. Download it today.

eBook | Next-Generation DNA Sequencing in the Clinic

eBook | Sponsored by: EMC Isilon | Published: October 7, 2013

There's no denying the power and promise of next-generation DNA sequencing (NGS) in the healthcare setting. Since 2005, when the first next-gen instruments hit the market, the field has exploded, and not surprisingly, companies have stepped in to fill unmet clinical needs. Here, we profile five businesses taking five different approaches to clinical NGS. Download today.

Bolstering Clinical Trials With Diagnostics

eBook | Sponsored by: Blinded Diagnostics | Published: August 26, 2013

This year has brought a bevy of partnerships between diagnostics makers and drug companies seeking to target experimental drugs to clearly defined patient populations. Download this eBook to learn how personal medicine will develop in today's world and help the patients of tomorrow.

Your Peers Expect a VDR. What Are You Using?

eBook | Sponsored by: Merrill Datasite | Published: July 22, 2013

While previously companies have kept their important paperwork in physical rooms, virtual data centers have recently become more popular. Download this ebook to learn how VDRs can make viewing classified documents safer and easier.

Collaborations in the Cloud

eBook | Sponsored by: Akamai | Published: July 15, 2013

Cloud-based technologies are proving to be useful within the life sciences industry. Download this ebook to learn how pharma and biotech companies are embracing efforts toward accessible and secure information for research collaborations.

Single Use Technology: From Bioprocess Convenience to Drug-Development Driver

eBook | Sponsored by: Catalent | Published: April 29, 2013

In order to accelerate the production of biological molecules, companies have been exploring disposable, single-use systems. Download this ebook to learn the impact and future use of single-use technologies, cost-saving opportunities, and challenges of implementing new drug development processes.

FierceBiotech Special Report | Foundations Fuel Risky Biotech Ventures

eBook | Sponsored by: Catalent | Published: March 25, 2013

Non-profits are taking larger roles in funding clinical trials and research. With their primary goal being finding cures, rather than financial gain, the influx of non-profit research donations may help accelerate cures and advanced research. Download now.

Tablets for Trials: Will Mobile Tech Make Development More Efficient?

eBook | Sponsored by: BioClinica | Published: March 18, 2013

With the clinical trial model as flawed as it is, pharma companies are turning to mobile technology as a way to increase success rate and drive down costs. So, what, if anything, can tablets and smartphones do to improve drug development? Download now.

Patient-Centric Drug Formulation Principles: Formulating Drugs for Children and the Elderly

eBook | Sponsored by: Aptalis Pharmaceutical Technologies | Published: March 8, 2013

How are drug developers and doctors tailoring prescriptions to patients? FierceBiotech outlines the principles and strategies for patient-centric drug development. Learn More.

Conversations with World-Class Biotech Innovators

eBook | Sponsored by: Catalent | Published: February 28, 2013

What elevates a researcher to the top of the industry? FierceBiotech profiled five prominent researchers and asked them how they garnered such success. Download for free today.

Special Report: China's Rise Drives Investment in Biotech Drugs

eBook | Sponsored by: Catalent | Published: January 22, 2013

The Chinese government's devotion to biotech has sparked major expansion efforts by some of the country's leading pharmaceutical players, also making it fertile ground for venture capitalists in the U.S. Click here to download the complete report today.

Special Report: Rare Disease and Orphan Disease Drug Development

eBook | Sponsored by: Catalent | Published: November 5, 2012

Drug developers are devoting considerable resources to rare indications and adopting some clever science to bring those orphan diseases home. To read more about the challenges and opportunities associated with bringing drugs for rare diseases to market, click here to download the complete report today.

Sterile Manufacturing of Semi- Solids and Liquids

eBook | Sponsored by: DPT Laboratories | Published: October 30, 2012

The role of sterility is a simple one—it is to protect people against infection and contamination. Vital steps and approaches in sterile manufacturing include employee training, process qualification and validation, processes and protocols for cleaning and decontamination, and methods to protect sterility and reduce contamination during processing.  Click here to download this eBook today.

FierceBiotech Special Report: Armed Antibodies Readied for War on Cancer

eBook | Sponsored by: Catalent | Published: September 29, 2012

For the drug developers looking to bring these products to market, ADCs represent the inevitable marriage of two sometimes hit-or-miss technologies, chemotherapy and antibodies, the next generation of anti-cancer compounds. In this Special Report FierceBiotech explores the potential and the challenges of the burgeoning field of ADCs.

The Right Fix: How Patient- Centric Data is Driving ROI and Revolutionizing the World of Pharmaceutical marketing

eBook | Sponsored by: IMS Health | Published: August 13, 2012

Advances in Anonymous Patient Level Data have empowered pharmaceutical marketers to refine their efforts to reach desired customers, accurately monitor the success of their campaigns, and ultimately generate greater ROI. Click here to download today.

Waiting for Guidelines, Will FDA Take the Reins of Laboratory-Developed Tests?

eBook | Sponsored by: Myraqa, Inc. | Published: May 21, 2012

A new set of FDA regulations, covering a field the agency has chosen not to supervise in the past, could be a danger on both sides. As many labs, test developers, consultants and FDA lawyers have said, it's the kind of regulation that threatens to stifle innovation with more government red tape. Click here to download.

Supplying Global Clinical Trials: Keys to Avoiding Costly Delays

eBook | Sponsored by: Catalent | Published: April 16, 2012

This FierceBiotech eBook provides expert analysis and industry insights to guide biopharma professionals that face the challenges of meeting strict timelines, selecting contractors and avoiding setbacks during the planning and execution of manufacturing partnerships for global clinical trials.  Download Now.

Trends in Enterprise Content Management in BioPharma

eBook | Sponsored by: OpenText | Published: March 19, 2012

This FierceBiotechIT eBook looks at how ECM has evolved, what the challenges to biopharma are, and how those challenges and obstacles are being met by a variety of ECM approaches. Download now.

Oral Drug Delivery Technologies: Tackling Clinical and Commercial Challenges

eBook | Sponsored by: Catalent | Published: March 12, 2012

This FiercePharma eBook examines Big Pharma's need for technology to give new life to old drugs, and potentially deliver their next breakthrough medicines. This report covers some of the market opportunities, business strategies, and key innovations in the oral drug delivery field. Register Today!

Academic and Pharma Partnerships: Tapping the Ivory Tower for the Next Blockbuster

eBook | Sponsored by: Merrill Datasite | Published: February 20, 2012

This FiercePharma eBook examines the changing relationship between Big Pharma and academia. Through interviews with both academic and corporate insiders, we gather perspectives from each side and address potential stumbling blocks. While there are pitfalls along the way, there is also great potential if the path can be navigated safely. Download today.

Including China in Drug Development Programs: Opportunities & Challenges

eBook | Sponsored by: Quintiles | Published: February 6, 2012

China’s market growth makes it an attractive target for biopharmaceutical development. FierceBiotech takes an in-depth look at both the opportunities and challenges that come with drug development in the world’s most populous country. Download PDF now.

Open R&D: Big Pharma Start Putting Collaboration Plans Into Practice

eBook | Sponsored by: Catalent | Published: December 10, 2012

There's no part of the business more in need of metamorphosis than R&D, and no one more convinced of it than pharma's movers and shakers. To read more on this topic click here to download this eBook today.