Since 1995, the principals of Crosby & Associates, AIA have been designing large, complex Pharmaceutical, Nutraceutical and Food & Beverage facilities throughout the United States, Europe, Asia and Central America.
In 2014, in response to the growth of the Medical Cannabis marketplace in the United States and Europe, Crosby & Associates assembled a team of expert cannabis Architects, Engineers, Planners, Cultivation professionals and Regulatory experts who are designing cutting edge cultivation, processing and dispensing facilities throughout the United States and Europe that are both high performance facilities and fully GMP compliant.
The Crosby & Associates team is providing expert assistance to a wide range of clients in the rapidly expanding cannabis marketplace. The Crosby & Associates team provides comprehensive, hands-on GMP Quality Compliance services to the pharmaceutical, biotechnology and cannabis industries. We have been providing pharmaceutical GMP consulting services to clients since 1995.
Since 2016 we expanded our GMP consulting practice to include our growing number of cannabis clients. We are now providing GMP consultancy services for many of our cannabis clients in the United States and the European Union.
Our Team provides GMP compliance services for new facilities and for existing facilities. The Crosby & Associates GMP compliance staff have deep experience in the industry and understands the tasks that will need to be completed to successfully bring our clients’ facilities into GMP compliance.
Our team is focused on your success.
How We Do It – A Service Approach
Our GMP compliance services are provided in three primary service categories:
● Building Facilities & Equipment
● Production & Processes
● Quality Systems
Depending on our clients’ specific needs, we can provide expert assistance in all the service areas, or in only one or two of the service categories listed above, as needed.
Prior to starting any project, we will work with our client’s team to clearly define the scope of our services, our client’s goals and objectives, the regulatory bodies having jurisdiction over the project and a timeline for completion of the services required.
Once engaged, we proceed with our work in a five stage process. Each stage of our work is planned to build on the results of the previous work stage. Once all stages are complete, our client will have a clear path to full GMP compliance.
Our team will work closely with our client’s team and other owner engaged consultants to assure the successful completion of the project.
Our five focused work stages are:
1. DEFINE REGULATORY FRAMEWORK
2. REVIEW EXISTING DATA
3. INSPECT/MONITOR/COLLABORATE
4. ANALYZE & EVALUATE
5. ISSUE FINAL REPORT
Whether your project is in the United States or in Europe, is new construction or an existing facility, our organized and in-depth approach to creating GMP compliance solutions will assure that your project will have a successful outcome.
The Phytos team is your best GMP compliance partner.
Our Team is focused on your success.