Biotechnology Documentation and IT Regulations Training, Compliance Best Practices and Standards
Biotech industry documentation requirements and IT regulations based webinars, in-person seminars, standards and best practices. Learn from renowned experts about FDA documentation requirements, IT and computer systems regulations for the biotech industry - ISO 9001:2000, FDA compliant, Compliant documentation, Technical writing, Electronic records, CTD, cGMP’s, cGLP’s, cGCP’s, Computer validation, Validation Master Plan etc…
You Recently Viewed
