End-to-End Regulatory, Compliance, and Clinical Trial Expertise in India
Supports the Complex and Highly Regulated Healthcare Industry. Meshayu Stands as One of the Reputed Healthcare Consulting Firm. Explore Our ServicesOur Expertise in Regulatory Compliance & Plant Design
We provide end-to-end solutions for regulatory approvals, compliance consulting, and plant design, ensuring seamless operations in the healthcare sector.
Plan Design and Development
(Pharmaceutical APIs and/or Pharmaceutical Formulations compliance to WHO-GMP/PICS/EUGMP/UK MHRA)
(Medical Devices and/or In Vitro Diagnostics compliance to MDR 2017/ EU MDR 745/746 and US 21CFR 820)
Pharmaceuticals formulation and Active Pharmaceuticals Industries
Various Regulatory Services concerning to the State Licensing Authorities (SLA)
Various Regulatory Services concerning to the Central’s Zonal Licensing Authorities (CLA-Zonal CDSCO)
Medical Devices and In-Vitro Diagnostics
Applications for Manufacturing Test license under Form MD 12 (Medical Devices/IVDs) – CDSCO
Applications for Manufacturing License under Form MD 9 (Medical Devices/IVDs) – CDSCO
Cosmetics
Applications for Manufacturing License under COS 5
Applications for Additional Product Approvals
Meet the Minds Behind Our Success.
Dip Joshi
(Corporate affairs / NPPA / CBN)
dipjoshi@meshayuconsultants.com
Hiren Patel
(MD / IVDs / New drugs & Clinical Trials)
hiren.meshayu@gmail.com
Piyush Patel
(Plan design / development (Turnkey Projects)
RND@meshayuconsultants.com