We are partners in multiple manufacturing facilities and are working on a smaller scale buildout in California at the moment. We are now at the stage where GMP certs are needed for the products that will be put forward.
I wanted to reach out, prior to initiating the process, to see if anyone has advice/pointers on the process in California.
Would suggest taking a look at the FDAs proposed Tobacco GMP rules, then at general Pharmaceutical Manufacturing cGMP
Its all basically SOPs, Training, and records of both.
Typically this needs to be compilied by your compliance officer, who is responsible for implementing and maintaining those 3 things. Often companies hire consultants to train their compliance officer, however a qualified one can be found and poached.
Shoot me a DM if you need any direct help, this is a field I’ve been focused on lately