SOP Request

PACT is now providing general facility SOPs upon request to assist you in developing your own cell processing facility SOPs. PLEASE NOTE that these SOPs are for INFORMATIONAL PURPOSES ONLY and therefore require validation by your own facility. Below are the SOPs currently available. Please click here to see the current list of SOPs under each category.
  • Cleaning Procedures
  • Deviation Management
  • Environmental Monitoring
  • Personnel Training
  • Quality Assurance/Quality Control
  • Quality Management
  • Regulatory/Clinical
  • Standard Operating Procedures (SOP): Development and Management
  • Validation

Once you have provided all required information, we will process your request as soon as possible. You should receive the SOPs you have requested in Adobe Acrobat format. Please confirm receipt of the SOPs by replying to the email. If the link above does not function properly with your email client, you may simply send us an email to the address below with the same information.

Click here to request one or more SOPs

*This will open an email window with an email request.

Association of Academic Biologics Manufacturers (AABM) is a cooperative network of non-profit academic based biologics manufacturers serving as a national resource to bring together clinical investigators with manufacturing capacity and expertise, develop and share facility operations expertise amongst members, provide quality, manufacturing and regulatory training opportunities, and hold annual meetings. AABM has assembled a library of SOPs that are available to registered members. The available SOPs cover such areas as facility operations, biological waste management, good documentation practices, document control, employee training policies, and gowning. Register to become a member or register your facility and receive access to these SOPs at There is no fee to register.

The Biopharmaceutical Development Program (BDP) at the Frederick National Laboratory for Cancer Research (FNLCR) provides resources and expertise for development of investigational biological agents. The BDP supports feasibility through development and Phase I/II cGMP manufacturing plus regulatory documentation. The BDP has over 300 documents online that are available free for any investigator, company, or group developing biopharmaceuticals. These documents are useful to scientific, clinical manufacturing, quality control and quality assurance professionals.