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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

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

Clinical Data Management Courses - PG Executive Diploma | IGMPI

Post Graduate Diploma/Executive Diploma in Clinical Data Management (CDM). Clinical data management (CDM) is the field which transforms raw data into consistent, accurate, reliable, meaningful trial output at a fair pric
https://www.igmpi.ac.in/clinical-data-management - 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

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

FDA Listing Inc. | FDA Compliance Solutions

FDA Listing Inc., a New York-based company, provides FDA registration, labeling compliance, and U.S. agents to food, cosmetic, drugs, and device industries.
https://fdalisting.com/ - 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

Drugs of Abuse Analysis with Urine Dip Drug Test Kits • Urine Drug Tes

Multi-Drug Screen Urine Drug Test Dip Cards are the most popular method to detect substance abuse by rapidly analyzing an individual’s urine for drugs and drug metabolites. Buy now at the lowest prices from a reliable so
https://www.buyatestkit.com/drugs-of-abuse-analysis-with-urine-dip-drug-test-kits/ - Details - Similar

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

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