Our Professional Services team can help you identify the problems areas of your controlled processes throughout all phases of pharmaceutical drug development and pharmaceutical manufacturing to drive new efficiencies and to promote transparency.
Valor has extensive experience in auditing vendors
against regulatory requirements. We have undertaken many different audits over
the years for many different systems in all areas of GxP. We focus on ensuring
that systems are adequately documented and validated. We also evaluate whether
systems are fit for their intended use and whether they are a good fit for our
Valor can assist in the preparation of SOPs that
support the ongoing activities of our clients in addition to providing guidance
for the implementation or revision of SOPs to ensure compliance with regulatory
requirements. We can also provide standard templates of SOPs, forms and
checklists developed in compliance with ICH guidelines, FDA CFRs, EMA
directives, Health Canada regulations and industry standards, We can provide this review as part of an ongoing Quality Assurance
oversight mandate or on an ad-hoc basis.
Valor experts in ISO certification provides a complete implementation service, taking customers from initial assessment to certification.