Care Pharma Consultant
Consulting firm focused on pharmaceutical quality systems, process simplification, productivity improvement and cGMP compliance. Services include cGMP auditing, quality consulting, training, validation/qualification and automation/digitization support for pharmaceutical manufacturers and suppliers.
Industries
Nr. of Employees
small (1-50)
Care Pharma Consultant
A / 502, F K Residency, Opp. Nutan Housing Society, Malarpura, Nadiad, Pin code: 387001, Gujarat, India.
Services
Comprehensive auditing services covering supplier/vendor qualification, contract manufacturer and third-party site audits, gap assessments, investigations, internal/QMS verification and regulatory compliance verification.
Advisory and implementation services for process simplification, productivity improvements, SOP/QMS setup, quality culture transformation and QA documentation.
On-site and virtual training across cGMP topics, validation, ISO and soft-skill/leadership programs tailored to client needs.
Comprehensive auditing services covering supplier/vendor qualification, contract manufacturer and third-party site audits, gap assessments, investigations, internal/QMS verification and regulatory compliance verification.
Advisory and implementation services for process simplification, productivity improvements, SOP/QMS setup, quality culture transformation and QA documentation.
On-site and virtual training across cGMP topics, validation, ISO and soft-skill/leadership programs tailored to client needs.
Expertise Areas
- cGMP auditing
- Quality management systems (QMS) implementation
- Process simplification and productivity improvement
- Quality culture transformation
Key Technologies
- Quality Management Systems (QMS)
- Computer System Validation (CSV)
- cGMP auditing methodologies
- Lean / 6S methodologies
News & Updates
Track record of completing more than 150 cGMP audits globally.
Assisted clients in successfully clearing EU-GMP, ANSM, US FDA, PICs and other regulatory audits.
Implemented SOPs and QMS for a sterile and non-sterile manufacturer with 100+ products.
Delivered QC productivity improvements including process simplification and low-cost automation implementations for multiple manufacturers.
Completed large-scale SOP simplification and global standard implementation across hundreds of SOPs for a life-science organisation.
Track record of completing more than 150 cGMP audits globally.
Assisted clients in successfully clearing EU-GMP, ANSM, US FDA, PICs and other regulatory audits.
Implemented SOPs and QMS for a sterile and non-sterile manufacturer with 100+ products.
Delivered QC productivity improvements including process simplification and low-cost automation implementations for multiple manufacturers.
Completed large-scale SOP simplification and global standard implementation across hundreds of SOPs for a life-science organisation.