P. R. Shah

About us

Rim Quality Systems undertakes total responsibility for Green Field Projects for Formulation and Bulk drug. We do innovation in pharma project with experienced technical team of pharmacist and engineers. We also help in UPGRADATION OF PLANT with minimum expense.

Rim Quality Systems is complete quality solution and management systems. It takes care for Total Documentation, Validation, Training, Preparation of Domestic/International regulatory audits and any other issues related to Quality System.

GMP AUDITS
We also conduct GMP Audits to monitor the compliance of GMP for Quality endeavors.

SOURCING
We also help in sourcing for ACTIVE PHARMACEUTICAL INGREDIENTS (API), Bulkdrugs & Contract Manufacturer for Formulation.

TRAINING
We provide total training for GMP / GLP / GWP / GEP / VALIDATION / STABILITY / DOCUMENTATIONS. We also provide Guideline for preparation of CTD / DMF / ANDA Documents.

Services We Serve

New Pharma Turnkey Projects

Master Plan.
Architectural and Structural Designing
Detailed Electrical Design
Designing for Utilities System
Fire Fighting and Safety System
Piping Engineering
Process Automation Design
Procurement assistance
Co-ordination with site contractor

Inquiry

Upgradation Of Pharma Plants

Master layout & submission drawings.
Project report including Cost of total project, Production capacity , operation cost.
utilities consumption
Project management- Follow up & coordination with various agencies up to completion of total project.
Provide guideline, Effective supervision , site meetings and trouble shooting
Designing for total utility system.
Modification of layout
Up gradation of utilities system & its designing.

Inquiry

Quality Management System

We provide guideline & training for QMS.
Guideline for total Documentation of Quality Systems.
Validation of Systems, Processes, Equipment, Cleaning.
Stability Profile for Product.
Preparation of Domestic/International regulatory audits.
Any other issues related to Quality System.

Inquiry

Value Added Services

SOURCING

We also help in sourcing for ACTIVE PHARMACEUTICAL INGREDIANTS (API), Bulk drugs & Contract Manufacturer for Formulation.

GMP AUDITOR

We also conduct GMP Audits to monitor the compliance of GMP for Quality endeavors and Investigation for Quality failure.

TRAINING

We provide total training for GMP / GLP/GWP/GEP/ VALIDATION /STABILITY/ DOCUMENTATIONS. We also provide Guideline for preparation of CTD / DMF / ANDA Documents.

FACILITY AUDIT CONSULTANCY

We also offer Facility Audit Consultancy which is important for clients who are planning to purchase an existing pharma unit. Our primary audit check points covered are as below: