Industries We Serve

Pharmaceutical formulation

We believe that design of finished dosage form facility is more of an art than just pure engineering and science. It requires a clear understanding of not only the processes but also requires consideration of current GMP regulation, statutory norms and special requirements of gowning, clean room concept, air filtration, water purification, man and material movement.

CPP has successfully completed many projects for sterile and non-sterile pharmaceutical facilities across India.

We have experience in setting up facilities for almost all the known dosage forms. These includes:

• Oral solid formulations
• Liquid syrup and suspensions
• Large and small volume parenteral
• Topical applications

API & Intermediates

CPP has experience in setting up facilities for pharmaceutical API (active pharmaceutical ingredients) and intermediates.

Expertise include:

• Setting up facilities in accordance with cGMP of local and international regulatory authorities.
• Revamping of existing facilities in accordance with cGMP and regulatory standards.
• Design and engineering of facilities for potent compounds including oncology, hormones, steroids, immunosuppressant’s and general segments etc.