Our Services

  • Qualified Person services as per Directive 2001/83EC

  • Interim QP services

  • Responsible Person (RP) services for GDP requirements as per Guideline 2013/C 343/01

GMP Audits for:​

  • Active Pharmaceutical Ingredients (ICHQ7)
  • Finished products (Directive 2003/94/EC)
  • GXP including GDP and artwork studios
  • ISO9001
  • Inspection Readiness

Training in areas such as: 

  • cGMP

  • Artwork origination GXP

  • Supply chain management

  • Bespoke in house training covering topics such as problem solving skills, CAPA & Quality Risk Management

  • Quality improvement programmes based on Kaizen and tailored to company requirements

  • Implementation of quality systems such as ISO9001 or ICHQ10 

  • Assist in attaining licences: MIA, ManA or WDA.

  • GXP auditing (gap analysis) for a pharmaceutical artwork studio and deployment of 'best practice' standard

  • GXP training appropriate for pharmaceutical artwork studios

  • Outsourcing artwork capability 

  • Sourcing and evaluating artwork systems providers

  • Pharmaceutical packaging design and patient information leaflet user testing (in collaboration with a CommQP partner company)

 

  • Market research and business development with Indian pharmaceutical and biotech companies

  • Provide access to MIA & WDA holders, GXP laboratories, GDP warehouses & pharmacovigilance specialists for companies wanting to market their products in the EU.

  • Supplier sourcing and supply chain management

  • Supply chain efficiency projects based on LEAN principles so delivering quality & cost benefits

Mukesh T Patel BSc(Hons) CChem MRSC CSci MCIPS
07831 398 653
mukesh.0001@yahoo.co.uk
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Registered in England

Company No. 8022888

Vat Registration No. 132072652