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Product Registration Services

MS Remedies have experts with decades of experience with product and process development and steer numerous project including several blockbuster products with reputed Pharmaceutical companies. With education and exclusive research and development experience, our experts provide Chemistry, Manufacturing and Controls (CMC), a robust and repeatability process from inception to development and support regulatory registration. We also serve private equity investors with due diligence audit for potential product for any market across the globe. Please contact MS Remedies Inc. at +1-647-229-7236, +1-905-901-2724 or info@MSRemed.com

 

We provide detailed Technology Transfer and Scale-up Master Plan, which paves a solid ground for success of your organization and future transfer or scale-up.

 

We help your organization with following activities:

-Chemistry/ Manufacturing/ Controls (CMC)

-Operational Excellence

-Facility Design

-Product Development

-Process Development

-Training and Certification

-Technology Transfer

-Process Scale-up

-Process Trouble-shooting

-Due Diligence Assessment

-Development Report

-Analytical Method Development

-Regulatory Filling

-Quality by Design (QbD)

-Process Analytical Technology (PAT) implementation

-Design of Experiment (DOE)

-Identification for Critical Process Parameter (CPP)

-Identification for Critical Quality Attribute (CQA)

-Defining correlation between CPP and CQA

-Specification Justification

-Manufacturing Design and Control

-Product Partnering, Out-Licensing, and In-Licensing

-Compliance

 

Contact MS Remedies Inc. at +1-905-901-2724, +1-647-229-7236 or info@MSRemed.com