Gallery List | Gallery
Order by Order by:
Business Directory
Results for Business Directory in Alabama 1 - 13 of 13
Understanding about the quality and regulatory aff

Understanding about the quality and regulatory aff


The Quality and Regulatory Affairs office is crucial connection between organization, products and regulatory specialists whose positive or
Ivdr classification – ce marking | operon strategi

Ivdr classification – ce marking | operon strategi


The New IVDR Classification necessary changes are compared with the previous In Vitro Diagnostics Directives structure Contact details –
Iso 15378 certification consultant – operon stateg

Iso 15378 certification consultant – operon stateg


ISO 15378 Certification is a quality assurance for primary packaging materials for medical products specific prerequisites for the
Iso 13485 medical device certification –operon

Iso 13485 medical device certification –operon


Operon Strategist is ISO 13485 consultant helps to create the documents for ISO 13485 certification. This includes the creation of the SOP,s
Clean room design consultant – operon strategist

Clean room design consultant – operon strategist


We as Clean Room Design Consultants, guide Medical Device manufacturers on supporting elements to maintain their clean room conditions
Medical device regulatory consulting

Medical device regulatory consulting


We provide Consulting Service for Medical Device Industry. Our team can advise you on every aspect of global standards and compliance
Medical device regulatory consulting services - op

Medical device regulatory consulting services - op


We provide Consulting Service for Medical Device Industry. Our team can advise you on every aspect of global standards and compliance
How to integrate usability into medical devices

How to integrate usability into medical devices


Integrate Usability into medical devices for a better risk based testing process that includes testing how easy simple and safe a medical
Indian healthcare scenario all set to change | med

Indian healthcare scenario all set to change | med


The new medical device rules which came into force from January 2018 has finally given the medical devices and in-vitro diagnostic
Get to know brief on multi-level design controls

Get to know brief on multi-level design controls


Multi-Level Design Control will permit medical device makers, and specifically, SaMDs, to more readily oversee segments or sub-parts by
Quality management systems (qms) certification - c

Quality management systems (qms) certification - c


The QMS is defined to help the streamline and reinforce the internal process, or procedure. The QMS certification is a planned method for
Us fda 21 cfr 820.30 design control requirements

Us fda 21 cfr 820.30 design control requirements


Operon Strategist the leading medical device 21 CFR 820.30 design control consultants have extensive experience with the practical
Are you preparing for the medical device single au

Are you preparing for the medical device single au


The Medical Device Single Audit Program permits an MDSAP perceived Auditing Organization to lead a single regulatory audit of a medical