- Quality Systems audits/assessments, pre-certification audits, Quality Systems implementations, process improvement, SOP development, work instruction and procedures development
- ISO certification assistance
- Corrective and Preventative Actions (CAPA) processes and systems services
- Device master record/technical files remediation
Τρίτη 15 Σεπτεμβρίου 2009
Pharmaceutical > Quality Systems
PHARMACEUTICAL PRODUCTS
Pharmaceutical manufacturers are faced with a continually tightening regulatory landscape. In fact, the EMEA initiatives focused on increased vigilance of pharma companies from supply chain through post-market surveillance. It is imperative that a proactive approach is taken to construct the robust quality and compliance infrastructure that the EMEA demands.
MeekSystems Corp. has been providing professional services to pharmaceutical companies since 2008. We have deep regulatory, quality, and technical experience that reaches across virtually all functional and technical areas including sales and marketing, manufacturing (whole & partial ), importation from third countries, laboratory, clinical, pharmacovigilance and supply chain (wholesale, retail, distribution ) management.
Our approach to every project creates a unique synergy between compliance objectives and results-oriented business goals.
The consequences of a reactive quality and compliance program have been promised by the EMEA to be far greater than the costs associated with building a solid quality and compliance infrastructure proactively. If this opportunity cost is too high for your organization, contact MEEKSYSTEMS CORP. right away to proactively face the EMEA's quality and compliance expectations with confidence.