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RxPharmatech360 Welcomes You
RxPharmatech 360 is an international pharmaceutical consulting company. RxPharmatech 360 has an extensive network of consultants from all different areas of expertise in pharmaceuticals. That helps companies to achieve their objective. We have associated auditors have extensive global experience in auditing.
- We offer services as single assignment or for long term.
- Our Ethics to support in such matter is with the aim of survival of the business /families. Who are associated with the affected sites.
- We assist and advice for a comprehensive CAPA to mitigate the deficiency that will be acceptable to any regulatory agency without any further query.
- Active support can be providing consideration the tight timelines to regain the license to operate.
- We are consultant that provide services to connect foreign manufacturer to regulatory environment of the USFDA/MHRA.
- Our team combines considerable experience in industry and our associates have exposure at FDA & EU with current regulatory technical knowledge to provide guidance.
Why Should You Consult Us?
Auditor with non-compliances on your site and Regulatory non compliances not resolve from long time can be very expensive to your business.
Investing in a cGMP consultant will pay for itself over and over again as you enjoy the systems that make the compliance easy.
- Save company’s product in the market.
- Resolving product failure issues or any product sustainability in question
- Identify and work out on root cause or causes and get accurate product manufacturing within the specified limit.
- Effective Report Writing to regulatory authority.
- Compliance for regulatory product approval
- Rectifying the Testing issues.
- Rectify and resolve the product stability issue.
- Effective Training system
- Settle the Pharmaceutical company’s environmental worries in concern to HVAC.
- Put things right when Water System is in question.
- Determine the Machines issues for better output.
- When product contamination is the concern.
- Determine the companies to get back their license in case of withdrawal.
- Product Design Control
- Inspection Readiness
- Site compliance to MHRA & USFDA
- Supplier and Vendor Audits
- Support for effective implementation of PQMS
- Implementation of Management and Employees involvement
- Compliance of Regulatory Guidelines
- Oral, Liquid and Parental Dosage Form with production, Quality and Engineering Excellence.
- Can assist your company to reduce the cost and time to the Market.
- Our services will continue long after our engagement is over.
- To advise on the continuous improvement of manufacturing processes
