_eqms-software-124-electronic-quality-management-software-124-electronic-qms-124-amplelogic.jpg "EQMS Software | Electronic Quality Management Software | Electronic QMS | AmpleLogic from cfr biotechnology Video Screenshot Preview")
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!)
⏲ Duration: 1 min 25 sec
✓ Published: 19-May-2020
✓ Published: 19-May-2020
Description:
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
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
Share with your friends:
Whatsapp | Viber | Telegram | Line | SMS
Email | Twitter | Reddit | Tumblr | Pinterest
Related Videos
_life-sciences-data-management-and-compliance.webp "Egnyte for Life Sciences helps leading biotechnology, medical device, and drug development companies innovate faster through seamless compliance and unified document management. This overview video showcases how Egnyte's data privacy, GxP compliance, audit, eTMF, workflow, and Quality documentation products help Life Sciences companies connect globally distributed teams and protect their content. nnEgnyte's security and governance features enable secure remote work and empower clinicians, lab re")
_fda39s-current-thinking-on-cgmp-compliance-for-phase-i-investigational-drug-and-biologic-products.webp "GlobalCompliance Panel")
⏲ 39 minutes 23 seconds 👁 1.2K
_what-is-21-cfr-820.webp "Medical Device Academy")
_gmp-compliance-for-biotechnology-and-pharmaceuticals.webp "ZEISS Microscopy")
_21-cfr-parts-210-and-211.webp "Compliance Insight")
_navigating-21-cfr-part-11-current-challenges-amp-future-trends.webp "Dive into the essentials of 21 CFR Part 11 compliance in just a few minutes! This video offers a succinct overview of the regulation that's critical for anyone in the pharmaceutical, biotechnology, and medical device industries. We break down the regulation's key objectives, including ensuring data integrity, system validation, and the authenticity of electronic signatures. Plus, we explore current challenges, innovative solutions, and the promising future trends that are shaping compliance stra")
_21-cfr-in-pharmaceuticals-part-1.webp "Syed Irfan Bukhari")
_life-sciences-data-management-and-compliance.jpg)
_fda39s-current-thinking-on-cgmp-compliance-for-phase-i-investigational-drug-and-biologic-products.jpg)
_what-is-21-cfr-820.jpg)
_gmp-compliance-for-biotechnology-and-pharmaceuticals.jpg)
_21-cfr-parts-210-and-211.jpg)
_navigating-21-cfr-part-11-current-challenges-amp-future-trends.jpg)
_21-cfr-in-pharmaceuticals-part-1.jpg)
![[+]](/images/menu.gif){kind=small}