2022 will be remembered as the year of innovation in Quality and Compliance for the Compliance Group Inc. We sponsored a series of webinars for the life sciences industry sharing the new FDA Guidance for CSA as well as introducing the updated GAMP 5, second edition guide. Compliance Group helped 30+ clients transition from CSV to CSA.
We continued to make major enhancements in our Quality and Document management solution while also launching our new Intelligent Training Management product into the market.
We are extremely proud of the positive contribution we made to the industry educating thousands of people on this new critical guidance’s. and we look forward to continuing helping, supporting, and educating the bioscience industry stakeholders with all FDA-related guidance and compliances in the upcoming year as well.
Here is the quick summary of 2022.
Top 10 Blog Posts of 2022
How iQuality helps to avoid FDA Warning letters?
FDA issues warning letters to avoid compliance. Warning letters are issued when the FDA finds that a company from the life science industry is out of its way with the regulatory standards.
ISO 9001 Document Control Checklist
ISO 9001 enables an organization to adjust the documentation as applicable as long as the overall objectives are met. The change, however, does not decrease the need for accurate documentation.
FDA 483 observations and Warnings 2021 Where can I find? What are the most common FDA 483 inspection observations?
Explaining the most common FDA 483 inspection observations. Where FDA 483 observation is a notice to the manufacturers who do not adhere to compliance with the regulatory guidelines, a warning letter is one step above the notice that the higher officials.
How to Validate and ease Compliances related to CSA and CSV in Medical Device Industry?
Explains about Compliance Validations related to CSA and CSV in Medical Device Industry
How Training Management System helps to ease the training in Life Sciences Industry?
An automated training management system facilitates the organization of a streamlined process with documentation for easy access, assignment, monitoring, and management
ISO 14971 Risk Management Plans for Medical Device Industry
Explains about Risks faced during product manufacturing in medical device industries
CAPA Software - What are the major functions of CAPA Management Software?
Explains about CAPA Functions in eQMS Software
Importance of Version Control in a Document Management System
Explains about Version Control in Document Management System
How can records and documents linking increase the level of quality?
Explains about Records and Documents linking in Quality Management System
Is CSA applicable to Shipping Validation?
Covers about Shipping Validation Process in Computer Software Assurance
TOP 5 Webinars Organized by Compliance Group Inc
This Webinar Covers about Case Studies Related to CSA Draft Guidance
This Webinar Covers about Establishing Appropriate Record Related to CSA Draft Guidance
FICSA Townhall Webinar Live from MDIC Office
This Webinar Covers the Applications of CSA in your organization
This Webinar Covers about Risk-Based Computer Software Assurance Framework for computers and automated data processing systems used by manufacturers for production and/or quality system purposes.
