Thermo Fisher Scientific Expands Steriles Manufacturing and Research Capabilities in Asia-Pacific Region
The regulatory environment for Cell and Gene Therapies is evolving at a rapid pace. Many companies, especially new and emerging ones, often lack the internal resources, or expertise to support regulatory filings. Companies need a partner who continuously monitors the changing regulations and has the capabilities to support them with their regulatory needs.
Learn how Patheon Viral Vector Services, with over 15 years’ experience, provides a comprehensive range of regulatory consulting services for the cell and gene therapy innovators.