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The editorial team of BioPharm International present their podcast series, covering all the hottest industry trends from protein expression to biosimilars and regulatory expectations.

Outsourcing Cell Based Potency Assays
During this podcast, we will discuss industry trends, regulatory expectations and strategies for outsourcing Cell Based Potency Assays. Watch now

Critical Aspects of Antibody-Drug Conjugates: Structural Characterization and Analysis
During this podcast, we will discuss delivering targeted therapeutic agents with greater selectivity and less toxic side effects. Watch now

Key Value Considerations for Growing BioPharm Product Pipeline. Part II
In part II of this BioPharm International interview, Tarja Mottram, CEO of Action for Results, focuses on "design for value" - a paradigm shift in how the industry measures and provides evidence for the impact of a product on healthcare outcomes. Posted Feb. 2012. Listen now

Key Considerations for Commercializing a Compound
Joerg Zimmerman, director of process development and implementation at Vetter discusses the need to think carefully about the commercialization efforts that must be applied to a compound under development. Posted Jan. 2012 as part of BioPharm International's Basic Training Drug Development series. Listen now

Key Biosimilar Development in a Virtual Biotech Environment - Part II
Biosimilar development is not about conducting breakthrough research. Rather, it is about hitting the ground running and pressing the fast-forward button by using existing technologies to ensure first-in-class market access. Posted Dec. 2011 as part of BioPharm International's Basic Training Drug Development series. Listen now

Biosimilar Development in a Virtual Biotech Set-up - Part I
In this article, the co-founder and CEO of Finox Biotech shares insight into their approach to biosimilar development. Posted Dec. 2011 as part of BioPharm International's Basic Training Drug Development series. Listen now

Finox Biotech's Anjan Selz discusses the need for strong product differentiation
In this final podcast of three, Anjan Selz, cofounder and CEO of Finox Biotech, denounces the destructive nature of focusing only on price in the biosimilar space. Posted Dec. 2011 as part of BioPharm International's Basic Training Drug Development series. Listen now

Finox Biotech's Anjan Selz on Meeting Regulatory Expectations
In this second of three podcasts, Anjan Selz, cofounder and CEO of Finox Biotech, discusses his company's interactions with EMA and FDA. Posted Dec. 2011 as part of BioPharm International's Basic Training Drug Development series. Listen now

Finox Biotech's Anjan Selz on Biosimilar Development
In this first of three podcasts, Anjan Selz, cofounder and CEO of Finox Biotech, describes how he decided to move away from the 'me too' approach to biosimilars and focus on product differentiation. Posted Dec. 2011 as part of BioPharm International's Basic Training Drug Development series. Listen now

The Future of Drug Design
In this final podcast of three, BioPharm International interviews Dr. Trevor Hallam, chief scientific officer at Sutro Biopharma, a company that has developed a cell-free system for protein expression. Posted Dec. 2011 as part of BioPharm International's Basic Training Drug Development series. Listen now

Future GMP Manufacturing Facility
In this second of three podcast interviews, Dr. Hallam, chief scientific officer at Sutro Biopharma, describes a future GMP facility for the production therapeutic proteins and peptides. Posted December 2011 as part of BioPharm International's Basic Training Drug Development series. Listen now

MicroRNA Drug Delivery
Balkrishnen Bhat, senior director and head of chemistry at Regulus, discusses core technology in microRNA drug delivery. Posted Nov. 2011 as part of BioPharm International's Basic Training Drug Development series. Listen now

Cell-free Protein Expression
Dr. Trevor Hallam, chief scientific officer at Sutro Biopharma, discusses a nontraditional approach for expressing therapeutic proteins and peptides. Posted Nov. 2011 as part of BioPharm International's Basic Training Drug Development series. Listen now

Alnylam Discusses RNAi Delivery
Alnylam Pharmcaeuticals, a company specializing in RNA-interference therapeutics, talks to BioPharm International's Amy Ritter about its RNAi delivery system and its early-stage clinical pipeline. Posted August 2011. Listen now

Should Pharma Invest in R&D or Search for External Drug Candidates?
Join Shire's Renee Cohen, Sanofi's Ray Jupp, Deutsche Bank's Barbara Ryan, Ken Kaitin of Tufts University, and Charlotte Sibley as they debate how pharma can find new drug candidates and refill the pipeline. Posted July 2011. Watch now

USP 2011 Symposium Preview
A series of videos from the US Pharmacopeia (USP) provides highlights of the 2011 USP Science & Standards Symposium on Biologics & Biotechnology, which took place Oct. 3-6, 2011, in Seattle in the US. Posted September 2011. Watch now

Vermont's Data Mining Law
Physician privacy vs. Rep Free Speech: Before the Supreme Court decides Sorrell v. IMS Health, find out what's at stake. Jody Fisher, vice-president of marketing for SDI and Frank Pasquale, the Schering-Plough Professor in Health Care Regulation and Enforcement at Seton Hall Law School, face off in this episode of Pharma Faceoff. Posted July 2011. Watch now

A Conversation with NIH Director Francis S. Collins
Director of the National Institutes of Health (NIH), Dr. Francis Collins, discusses NIH's efforts to improve global healthcare, including an update on the human genome project, a focus on infectious and rare diseases in the developing world, and R&D grants for small businesses. Podcast interview by Sr. Managing Editor Angie Drakulich, as part of the 2011 BIO Convention and BioVentures for Global Health Partnering for Global Health Forum. Posted June 2011. Listen now

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