| 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
|
Vial Inspection & Sterilization |
