| ATS capabilities:
- Automation in
Aseptic & Isolated Environments
- Flexible Packaging
Systems and
Sub-systems
- Pharmaceutical
Production
Line Integration
- Automation for Drug Delivery Device Manufacturing
- Order Fulfillment and Complex Logistics
- Industrialized Biotechnology
Automation
Client Services Model
ATS engineers provide a full range of services, including
automation analysis and modeling, concurrent engineering,
proof-of-concept, and prototyping. Our goal is full
support of all automation needs from concept to turnkey
installation, training and support.
Qualification & Validation
ATS has broad experience in developing detailed
documentation based on each customer’s URS and
MVP processes. ATS is ISO 9001:2000 registered and ISO
13485 & FDA GMP 21 CFR § 210, 211, 820 compliant
Security & Counterfeit Protection
To combat the rise in counterfeit pharmaceuticals, ATS can offer customers a high contrast marking system that permanently embeds text, logos, lines and 2D bar codes into glass vials or products, so that end users can verify that the product originated in the intended pharmaceutical company’s factory.
|
Vial Inspection & Sterilization |
