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Structured Product Labeling, Structure Product Monograph Software

Freyr SPL/SPM is cloud hosted and On-premise software that supports in electronic drug registration listing management, Labeling Management, PI submission in SPL/SPM Format with Automated notification updates.
https://www.freyrsplspm.com/ - Details - Similar

Regulatory Affairs Compliance and Product Registration

FDA, EMA, Regulatory Affairs, Regulatory Consultants, Market Authorization, Pharmaceutical,Drug,Registration,Biotech,Medical Device,Pharmacovigilance, 501k
https://patternofusa.com/ - Details - Similar

FDA Registration - FDA Certificate - FDA Agent

FDA registration is the basic requirement for domestic and foreign establishments that manufacture or market food, drug, API, medical devices, or cosmetic products in the USA
https://www.fdahelp.us/ - Details - Similar

Institute of Good Manufacturing Practices India | New Delhi | IGMPI

IGMPI offers regular online learning programmes in Good Manufacturing Practices, Quality Assurance and Quality Control, GLP, IPR, Pharmacovigilance and CEP.
https://www.igmpi.ac.in/ - Details - Similar

Accreditation and Awards | IGMPI

IGMPI offers regular online learning courses in Good Manufacturing Practices, Quality Assurance and Quality Control, GLP, IPR, Pharmacovigilance and CEP.
https://www.igmpi.ac.in/affiliations-and-accreditation - Details - Similar

About Us - Institute of Good Manufacturing Practices Delhi, Noida, Vad

IGMPI offers regular or online learning programmes in Good Manufacturing Practices, Quality Assurance and Quality Control, GLP, IPR, Pharmacovigilance and CEP.
https://www.igmpi.ac.in/about-us - Details - Similar

Regulatory Services in Brazil, ANVISA, Brazil Regulatory Partner, ANVI

Freyr provides regulatory services and solutions in Brazil to comply with ANVISA for pharmaceuticals, medical device, cosmetics and food supplement manufacturer companies.
https://www.freyrsolutions.com.br/ - Details - Similar

21 CFR part 820 - Medical Device GMP

The GMP requirements are described in 21 CFR Part 820, which are similar to international standard ISO 13485
https://www.fdahelp.us/21_CFR_820.html - Details - Similar

21 CFR Part 211 - Hand Sanitizer and Drug GMP Requirements

Hand sanitizer and other Finished Pharmaceutical manufacturers in the USA and foreign manufacturers who distribute their pharmaceutical products in the USA are required to comply with GMP regulations
https://www.fdahelp.us/gmp.html - Details - Similar

Top Translation Company|ISO 9001:2015, ISO 17100:2015 & ISO 27001:2013

With over 17 years of experience in helping businesses worldwide to find perfect Language Translation solutions.
http://itranslationworld.com/ - Details - Similar

Your Ad Here & Hundreds of Other ISEDN Engines & Directories- $3/Month or Less

Your Ad Here & Hundreds of Other ISEDN Engines & Directories- $3/Month or Less

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