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www.joharidigital.com
Johari Digital Healthcare ltd.
Johari Digital is a global medical device manufacturing company with 40+ years of expertise in medical device manufacturing. The manufacturing facility is in compliance with MDSAP, ISO 13485:2016 and FDA (21 CFR 820) standards and processes. Their services range from design to development, electronics and mechanical engineering, prototyping, system integration, packaging and supply chain. Additionally, Johari also helps clients with regulatory and compliance support to quickly take their product
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globe.gotsm.com
GMP Training: GMP Audit,EU GMP,FDA cGMP,FDA Certification,GMP Consulting,GMP compliance ,FDA Program,Globepharm Consulting
30 years world-wide pharaceutical industry expertise in all aspects of GMP compliance and quality assurance. We know the FDA and we know what it takes to comply with GMP regulations
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elearning.globepharm.org
GMP Training: GMP Audit,EU GMP,FDA cGMP,FDA Certification,GMP Consulting,GMP compliance ,FDA Program,Globepharm Consulting
30 years world-wide pharaceutical industry expertise in all aspects of GMP compliance and quality assurance. We know the FDA and we know what it takes to comply with GMP regulations
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qualitysys.com
Compliance Management Software, Quality Management Software - IBS America
IBS is a leading provider of enterprise Compliance Management Software that helps organizations comply with a range of standards, including ISO 9001:2000, ISO/TS 16949, ISO 13485, ISO 14000, OHSAS'000, SOx, and FDA 21 CFR Part
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dickinsonautocon.com.au
Dickinson Autocon Systems - Leaders in batching systems and pharmaceutical manufacturing
Manufacturing information systems, automation and electrical services for a wide variety of industries. Feasibility, design, development, manufacture, installation and support, employing engineers from diverse backgrounds and disciplines, led by astute pr
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qaracc.com
QA/RA Compliance Connection, Inc
QA/RA Compliance Connection, Inc. Quality Assurance and Regulatory Affairs consulting services and training company. Provide asssessment, gap analysis, development, compliance, implementation to ISO 9001, FDA Quality System Regulation (QSR) 21 CFR 820, IS