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Medical Device Process Validation Services In North America
7 services found
Manufactured by:BMP Medical based inSterling, MASSACHUSETTS (USA)
BMP Medical offers full medical device process validation services for all of our customers. We will work individually with a project manager and your team to develop a validation master plan for your project. The plan can range from simple go/no go to a full IQ/OQ/PQ protocol. ...
by:STEMart based inShirley, CALIFORNIA (USA)
Cleaning is defined as removal of soil residues with manual or automated method. It is always the first and necessary step in reprocessing of reusable medical device. ...
Manufactured by:Biorep Technologies, Inc. based inMiami Lakes, FLORIDA (USA)
Before you can bring a critical medical device to market to help enhance – and save – lives, you need to be certain it’s right and ready. Along with a commitment to absolute quality standards, our medical device contract manufacturing offers rigorous process validation. ...
by:EMSAR based inLake St Louis, MISSOURI (USA)
CSA Soliance partners with leading equipment manufacturers to provide validation (IQ/OQ/PQ) services for equipment, instrumentation and software. Pharmaceutical, biopharmaceutical and medical device companies must maintain validation programs that ensure their equipment is qualified for use. These programs are costly maintain in house, leading many companies to request this service from their ...
by:ALS Environmental based inHouston, TEXAS (USA)
At ALS our Pharmaceutical Division is a provider of testing services to the Pharmaceutical and Healthcare industries in Australia, Europe and Asia. Committed to exceeding customer expectations we are able to provide high quality solutions across a range products, including human and veterinary products, intermediates and raw materials. Testing is conducted according to international standards ...
by:Life Science Outsourcing, Inc. based inBrea, CALIFORNIA (USA)
The medical device packaging design, testing, and validation process can be intricate and time-consuming, facing intense regulatory scrutiny and often being the largest cause of FDA recalls. Starting medical device packaging validation too late in the design ...
by:HingeClinica based inPrinceton, NEW JERSEY (USA)
HingeClinica is a world class partner for Medical Device services. We render End to End Medical device MDR compliance and Regulatory services, Clinical trial, Pharmacovigilance services to Medical Devices industry. Our Medical Device team has extensive experience in working with US FDA, EMA, PDMA, SFDA, Health Canada, DCGI and ROW, regulatory Submissions and ...