CIP/SIP, Cleaning Validation, and Risk Assessment Services for Pharmaceutical Manufacturing
Optimize Cleaning Processes
Expert CIP/SIP Design, Implementation and Monitoring Services
Just as cleaning has been a core part of Hyde's business since our founding in 1993, so too has been the accompanying science.
Hyde integrates cleaning science into every phase of your program, from developmental studies to hydraulic balancing and cleaning cycle development to cleaning validation and ongoing monitoring.
Regardless of which phase of your cleaning program requires attention, Hyde has a team of experts to provide support.
Experts in providing tailored solutions from concept to operational systems.
Analytical Laboratory
Ensure methods are validated and your cleaning program is backed by data, with access to the best in the business.
Method Validation
Recovery Studies
Cleaning Optimization
MACO Limits Determination
CQV Services
Commissioning, Qualification and Validation. Offering complete support across all industries we serve, spanning from black utilities to purification systems.
Master Planning
Risk Based Approach
Owners Representation
Paperless Validation
Engineering
Skilled at taking your project from concept to operation systems.