The Pharmaceutical, Life Science, Healthcare and Clinical research organizations (CRO) all require to face the complex task of meeting all FDA regulatory compliance requirements including 21 CFR part 11 and other ISO compliance standard and various regulatory authorities of various countries. From discovery to clinical trials to final delivery of product to the patients, need assurance of quality, safety and efficacy. Cost incurred in getting FDA consent is huge so delay in final delivery of product means lost revenue.
- Home
Company
About us
Corporate Maxim
Resources and Downloads
Careers
Technologies
Microsoft Practices
SAP/Open Source Practices
Mobile
Web
Digital Transformation
Services
Consulting
Industry Focus
Solutions
Supply Chain and SD
Sales Force and CRM
Drug Safety and Pharmacovigilance
Drug Dossier Management
Enterprise Quality Management
Digitization of Clinical Research
Manufacturing
Others
Contact us