Our team with several years of experience in GMP industries knows each and every aspect of GMP. In any GMP issues our professionals can advise for compliance. Our team of consultants will assist clients to avail new technologies and processes cost-effectively in compliance with cGMP. Our consultants can help manufacturers, importers, packagers to gain establishment license and site license in Canada/USA. Our Quality Assurance and Regulatory consultants are capable to assist several companies for identifying or remediating gaps, support to maintain global standards and cGMP requirements. LLC Laboratories and their associated consultants can assist in a wide array of FDA regulated industries such as pharmaceuticals, nutraceuticals, cosmetic, medical device, specialty chemicals-manufacturers, importers, contract packagers, distributors and wholesalers for quality and compliance.
Our aim to serve our clients with phenomenal consultancy services and useful cGMP support. We aim to serve our clients by providing effective cGMP support.
Our cGMP consultancy service portfolios including-
- cGMP assessment of production facilities and Quality system
- Third party audits of suppliers and contract manufacturing facilities
- Review and preparation of Quality Agreements
- Training program on GMP for staff and management
- Document and data review of Quality control testing
- Document design and control
- Change control processes document preparations
- Corrective and preventive action plan documentation
- Quality control, product release and quality assurance
- Addressing GMP audit observations
We offer Regulatory Affair services for Establishment license, medicinal product application and product registration in Canada, USA, Europe and Emerging markets.