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We can work with your existing Quality Management System or assist in designing and implementing new systems. We will audit to assess compliance and to help assure the integrity and robustness of your data and systems.

Non-regulated?

Organisations undertaking scientific research not currently governed by these regulations or guidelines can also benefit from our services.

 

Assessment of internal standards, establishment of quality management systems and regular review can lead to improvement in productivity and efficacy in the research laboratory, benefiting researchers and their sponsors financially, in patent protection and in timely achievement of project milestones.

Assurance Activities
Quality Assurance

Handy Consulting Ltd provides auditing and consultancy services to aid assessment, monitoring and improvement of compliance to the requisite regulations governing pharmaceutical and scientific activities.

Regulatory Frameworks

Good Clinical Laboratory Practice (GCLP)

Good Pharmacovigilance Practice (GPvP)

Good Clinical Practice (GCP)

Good Distribution Practice (GDP)

Good Manufacturing Practice (GMP)

ISO

 

Feedback from clients

 

“Thanks for this excellent piece of work.” A global pharmaceutical company.

 

“It is clear that you conducted a thorough and comprehensive audit on our behalf.” An international research & development organisation.

 

“Louise conducted a very professional audit. The feedback and advice we received will be beneficial to our improvement program overall, and is much appreciated.” A global research and development laboratory.