These standards are strict guidelines in place to ensure that pharmaceutical, biotech, and medical device manufacturing processes are consistently producing products that meet quality standards.
While we help you with designing your facility as per GMP guidelines, the compliance certifications are done by the relevant GMP authorities.
Designing manufacturing facilities, cleanrooms, and laboratories that comply with GMP guidelines. The design must incorporate the necessary features to minimize the risk of contamination, such as controlled environments, air filtration systems, and proper waste management.
Designing of specialized equipment and systems used in manufacturing processes. The equipment must be designed to ensure that it meets GMP standards, is easy to clean, and prevents contamination.
Creating manufacturing processes that comply with GMP guidelines. This includes the selection of raw materials, the creation of Standard Operating Procedures (SOPs), and the development of a Quality Control system.
Validation and qualification services ensure that the manufacturing process, equipment, and facility comply with GMP standards. Validation and qualification activities include testing, verification, and documentation to ensure that the process is reliable, consistent, and repeatable.
