_gmp-compliance-for-biotechnology-and-pharmaceuticals-preview-1.jpg "GMP Compliance for Biotechnology and Pharmaceuticals from cfr biotechnology Video Screenshot Preview 1")
Gallery_gmp-compliance-for-biotechnology-and-pharmaceuticals-preview-3.jpg "GMP Compliance for Biotechnology and Pharmaceuticals from cfr biotechnology Video Screenshot Preview 3")
Gallery_gmp-compliance-for-biotechnology-and-pharmaceuticals-preview-hqdefault.jpg "GMP Compliance for Biotechnology and Pharmaceuticals from cfr biotechnology Video Screenshot Preview hqdefault")
GalleryPlay Video:
(Note: The default playback of the video is HD VERSION. If your browser is buffering the video slowly, please play the REGULAR MP4 VERSION or Open The Video below for better experience. Thank you!)
Jump To Video Parts
⏲ Duration: 3 minutes 9 seconds
👁 View: 349 times
Play Audio:👁 View: 349 times
Description:
ZEISS Microscopy
ZEISS Microscopy
Share with your friends:
Whatsapp | Viber | Telegram | Line | SMS
Email | Twitter | Reddit | Tumblr | Pinterest
Related Videos
_fda39s-current-thinking-on-cgmp-compliance-for-phase-i-investigational-drug-and-biologic-products.webp "GlobalCompliance Panel")
⏲ 39 minutes 23 seconds 👁 1.2K
_21-cfr-parts-210-and-211.webp "Compliance Insight")
_chapter-three-biotechnology-part-2.webp "Science for all exams SST SPSC STS IBA NTS PTS OTS FPSC.")
_cmc-considerations-for-biotechnology-product-development-a-regulatory-perspective.webp "U.S. Food and Drug Administration")
⏲ 56 minutes 24 seconds 👁 6.6K
_chapter-three-biotechnology-part-1.webp "Science for all exams SST SPSC STS IBA NTS PTS OTS FPSC.")
_preserving-data-integrity-21-cfr-part-11-compliance-and-osmolality-as-a-process-parameter.webp "Labroots")
⏲ 55 minutes 42 seconds 👁 1.6K
_21-cfr-210-211.webp "Compliance Insight")
_eqms-software-124-electronic-quality-management-software-124-electronic-qms-124-amplelogic.webp "AmpleLogic EQMS software for life sciences is a web based quality management system which includes CAPA, Change Management, Customer Complaints, Deviation Management, Audit Management, Vendor Qualification, Out of Specification (OOS), Out of Trend (OOT), Document Management and Learning Management etc.nnAmpleLogic Electronic Quality Management Software enables you to comply with US FDA (21 CFR Part 11), MHRA, EU Annex 11, TGA, ISO and other applicable regulation standardsnnAmpleLogic eQMS softwa")
⏲ 1 min 25 sec ✓ 19-May-2020
_fda39s-current-thinking-on-cgmp-compliance-for-phase-i-investigational-drug-and-biologic-products.jpg)
_21-cfr-parts-210-and-211.jpg)
_chapter-three-biotechnology-part-2.jpg)
_cmc-considerations-for-biotechnology-product-development-a-regulatory-perspective.jpg)
_chapter-three-biotechnology-part-1.jpg)
_preserving-data-integrity-21-cfr-part-11-compliance-and-osmolality-as-a-process-parameter.jpg)
_21-cfr-210-211.jpg)
_eqms-software-124-electronic-quality-management-software-124-electronic-qms-124-amplelogic.jpg)
![[+]](/images/menu.gif){kind=small}