State-of-art Manufacturing Facilities

The another things which makes Pacific India ideal among the parties in Pharma industry for third Party Manufacturing is its state-of-art manufacturing facilities. We are fully integrated with advance machinery and opt modern technology for manufacturing of medicine. Our Manufacturing unit is certified by WHO, GMP and ISO. Apart from these, our manufacturing place consists of following facilities: QC lab, R&D analytical testing and R&D manufacturing Facility. We have clinical packaging and warehouse to carry our further activities after manufacturing medicine. Licenses (includes Schedules I-V) FDA registration State licenses (Manufacturing and Wholesale) DEA licenses (Manufacturing, Import, Export & Wholesale)

Third Party Pharma Manufacturing

Quality Assurance for the entire product along with clinical trial and lab tastings Help in creating trademark as well as choosing brand name. (If required) Guidance in selecting packaging designs along with packaging material Procurement. Introducing new and innovative molecules 1sttime supply will execute in 40-45 days. In case of repeat supplies, they will be execute within 20-25 days. Our job is not done at only manufacturing pharmaceutical products. Being a leading name in pharmaceutical sector we ensure to provide best services from our end to our business partners. Apart from this we try to keep pace with the changing trends and requirements in the pharmaceutical industry.