SWISS PARENTERALS LTD | SWISS PARENTERALS LTD UNIT 1

The CDMO is a third-generation family business with a deep history in the sterile injectables industry.

Founded in 1986 as a trading house, the company transitioned into a full-fledged manufacturing enterprise in 1999. This pivotal moment solidified our commitment to providing high-quality sterile pharmaceutical products.

Today, as a leading provider of sterile pharmaceutical manufacturing services, we operate a state-of-the-art facility in Ahmedabad, India, strategically positioned for global reach. Our dedication lies in delivering high-quality, safe, and effective sterile products that meet the stringent requirements of our clients.

Our site encompasses three distinct manufacturing blocks, dedicated to producing a range of small-volume parenteral:

Block A, established in 1999, houses production lines for a diverse array of sterile products including Ophthalmic Drops, Pre-filled Syringes, Sterile Eye Ointments, Ampoules, and Inhaled Anesthesia.

Block B, constructed in 2019, features lines for Liquid Vials and Lyophilization, Liquid Ampoules, and Sterile Dry Powder filling.

Block C, also built in 2019, serves as the hub for our Quality Assurance, Quality Control, and Administration departments.

1 Block A

Inhaled Anesthesia, Ophthalmic Drops, Pre-filled Syringes and Sterile Eye Ointments, Ampoules

2 Block B

Liquid Vials + Lyophilization, Liquid Ampoules, and Sterile Dry Powder filling

3 Block C

Quality Assurance, Quality Control, and Administration departments

Short description of the site and blocks:

Block A:

This block manufactures inhaled anesthesia, eye drops, eye ointment, and liquid ampoules.

The ground floor houses the eye drop line, pre-filled syringe (PFS) line, liquid ampoule line, manufacturing area, day store raw material (RM) store, and packing area.

The first-floor houses liquid inhalation (anesthesia), sterile ointment, and service areas such as the water system.

Block B:

The ground floor includes the dry powder line, liquid ampoule line, liquid vials with lyophilizers, packing line, entry airlocks for the sterile area, manufacturing area, and autoclave area.

The first floor houses the raw material (RM) store, vials/ampoules store, finished goods (FG) store, water system, PSG, MEDS, compressed air, and nitrogen generation plant.

The second floor includes bung stores, flip-off seal stores, sterile water for injection and diluents store, secondary packaging material store, and printed label store. Finished goods area and reject room.

Block C:

This block contains the Quality Control Labs, Quality Assurance Office, and support teams for purchase and administration. The building is designed for optimal functionality and includes three floors, each dedicated to specific functions.

Ground Floor: The ground floor contains the Director´s Cabin, the Quality Assurance team, the Purchase and Admin team.

First Floor: The first floor contains the Quality Control labs, which are divided into chemical and microbiology sections.

Second Floor: The second floor contains the stability chambers, where samples are stored under controlled conditions to assess their long-term stability. It also includes an area for retaining samples for future reference and document storage for recordkeeping