Quality Operations Procedures for Pharmaceutical, API, and Biotechnology (Repost)
Quality Operations Procedures for Pharmaceutical, API, and Biotechnology By Syed Imtiaz Haider, Erfan Syed Asif
2012 | 584 Pages | ISBN: 1439886903 | PDF | 3 MB
2012 | 584 Pages | ISBN: 1439886903 | PDF | 3 MB
To stay in compliance with regulations, pharmaceutical, medical, and biotech companies must create qualtiy SOPs that build in the regulatory requirements into actions and describe personal flow, internal flow, flow of information, and processing steps. Quality Operations Procedures for Pharmaceutical, API, and Biotechnology and the accompanying CD-ROM take into account all major international regulations, such as FDA, EU GMP, cGMP, GLP, PDA technical monographs, PDA technical reports, PMA concepts, journals of PDA, GCP, and industry standard ISO 9000, to be in compliance with documentation guidelines. No other resource deals exclusively with the key elements of quality control and quality assurance procedures for pharmaceutical operations and provides hands-on templates to be tailored to achieve global regulatory compliance.