Manufacturing Capabilities
Purpose-Built Manufacturing for Critical Healthcare Products
Our Manufacturing Process
Controlled Manufacturing. Reliable Results.
1
Material Receipt
Incoming materials are received, identified, documented, and handled according to established procedures.
2
Verification
Materials undergo applicable checks before being released for manufacturing use to avoid problems.
3
Sterile Processing
Products move through controlled processing stages designed to maintain appropriate product quality and sterility.
4
Product Filling
Products are filled using controlled filling processes appropriate to the product format and structure.
5
Inspection
Filled products undergo applicable inspection and quality checks, making sure the quality is high.
6
Packaging
Products are packaged and labeled according to approved specifications and requirements.
7
Quality Review
Manufacturing and testing documentation undergoes appropriate review before product release.
8
Product Release
Products are released according to established quality standards and regulatory procedures.
Manufacturing Traceability
Traceability is an important part of pharmaceutical manufacturing.
Our manufacturing approach includes:
- Raw materials
- Manufacturing batches
- Equipment and processing
- In-process controls
- Laboratory testing
- Packaging materials
- Finished products
- Quality review
Manufacturing Infrastructure
Modern facilities designed to support safe and consistent manufacturing.
Our manufacturing environment can include:
- Controlled cleanroom areas
- Aseptic processing areas
- Formulation suites
- Sterile filling lines
- Packaging areas
- Quality control laboratories
- Material storage areas
- Temperature-controlled storage