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"Why Biotech Sponsors Need Outside Support: IRB, IBC, DMCs, and EACs"

When the fate of your company hangs in the balance, you need expert guidance to navigate the complexities of biotechnology development and to make informed decisions.

Emerging biotechnology companies must navigate the complexities of the development and approval process for drugs, biologics, and devices – often with no previous experience. Do they need an IBC? An EAC? Can they find partners who understand their therapeutic area?

Sometimes the fate of the company, not just the product, hangs on the right answers to such questions. With limited pipelines and significant market pressures, these companies often have just one shot at a successful study. Most vendors lack the necessary therapeutic and scientific expertise to navigate the complex development landscape, so the selection of the right partner is critical. Without proper guidance, a biotechnology company faces significant risk to study and investor timelines.

Fortunately, in WCG’s whitepaper, “Why Biotech Sponsors Need Outside Support: IRB, IBC, DMCs, and EACs,” WCG addresses these crucial topics so biotechnology companies can move studies forward, faster. By downloading this whitepaper, you will:

• Understand when an IRB and IBC are required for a study.
• Gain the tools to accelerate your studies with the right approach to Study Review.
• Discover how to identify the right scientific review partner to ensure the integrity and quality of your clinical trials.

Claim your free whitepaper today.

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