- Home
- Services
- usa new jersey
- risk assessment
Show results for
Refine by
Risk Assessment Services In Usa New Jersey
6 services found
Manufactured by:Pharmadule Morimatsu AB based inNacka, CHINA
We can provide the following services: GMP audits. GAP analysis. Validation Master Plan. Commissioning, Qualification and Validation. GMP Risk Assessment and Control Strategies. Design Qualification. Quality Management System development and implementation. GMP consultancy and ...
by:Excelra based inIselin, NEW JERSEY (USA)
Our integrated IT services and bioinformatics expertise accelerate drug discovery and improve patient outcomes through bespoke scientific application ...
by:Xybion Corporation based inPrinceton, NEW JERSEY (USA)
Computer Systems Validation, Testing, And Compliance Services: If you are seeking computer system validation experts, look no further. Xybion has demonstrated expertise validating computer programs for all types of regulated businesses in the energy, transportation, financial services, and life sciences (including FDA-regulated businesses such as pharmaceutical and medical device manufacturers, ...
by:Ascendia Pharmaceutical Solutions based inNorth Brunswick, NEW JERSEY (USA)
In the intricate landscape of biopharmaceuticals, development timing is a critical factor that can significantly impact the success or failure of a drug. Saving time can mean the difference between being first to market for a new drug class or a first-to-file ...
by:Auspex Diagnostics based inWarren, NEW JERSEY (USA)
Since no two patients are the alike, it is crucial that patients learn as much as possible about their tumor to determine the most suitable treatment plan. The test looks at the unique tumor gene expression data and compare it to our proprietary database to assess the risk that the individual’s cancer will return after the surgery and the efficacy of ...
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 ...