CAPA is a part of quality management system of an organization and that can identify and eliminate the nonconformances. If you are looking out for best CAPA management system in manufacturing industry then Qualityze CAPA management system in the best one to be considered. Qualityze CAPA Management System is capable to do investigation and that can eliminate the quality problems and preventive action is to avoid recurring risk.
Resolve quality related issues with the help of Qualityze CAPA Management software in industries such as healthcare, pharmaceutical, aerospace, automotive etc.
In healthcare and pharmaceutical industries quality management is risky one and it can be managed by CAPA management software. Qualityze CAPA management software has inbuilt powerful analytical and reporting tools so that it’s very easy to take simple corrections.
Many professionals in the regulated industries need professional trainings from time to time for a number of reasons. They need to get trained to fill their learning gaps. These gaps could result from a lack of complete clarity of the latest or existing regulatory updates, or due to insufficient exposure to the different knowledge areas of their profession.
V Group Introducing in-depth information about CAPA, Root Cause Analysis, and Risk Management under the Pharmaceutical domain and describes the quality procedures required to eliminate the causes of an existing nonconformity and to prevent recurrence of nonconforming product, processes, and other quality problems.
Introduction Healthcare professionals are always in situations where they have to think fast and process an array of diagnostic test results, medications and past ...
Presented by Carolyn Albertson Gunter Frey Member, SG3 NEMA Medical device manufacturers are generally required to have a quality management system as well as ...
Best Practices: Integration of Risk Management and Corrective and Preventive Action Presented by: Norman L. Collazo Worldwide Director of Strategic Quality
This webinar will define what is the US FDA's expectations for proper laboratory practices, systems, equipment usage, and documentation / record-keeping. It will evaluate the requirements for how basic Quality Management System (QMS) expectations/requirements are addressed in the lab environment. The webinar with evaluate pharma GMPs and 21 CFR 58 and associated regulations to see how the GLPs can be implemented in the real world to achieve FDA requirements and ensure the accuracy and repeatability/reproducibility of lab results.
Pharmaceutical manufacturers are under continuous pressure to remain competitive while meeting the stringent regulatory manufacturing requirements. These manufacturing requirements range from simple electronic record keeping to complex data assuring consistently the reliability of the manufacturing processes, equipment and people’s training, raw material quality, sampling plans, root-cause-analysis, product’s deviations, etc. Atachi Systems’ experience in deploying MES for pharmaceutical manufacturing companies for several years in a row is a testimonial on its own. Put simply, Atachi Systems understands the importance of deploying an MES system that is strategic to its core manufacturing requirements, yet cost effective to maintain and run for years to come! Our clients call it the Atachi Advantage.
GlobalCompliancePanel, the flagship brand of NetZealous LLC, a well-known provider of professional trainings in the regulatory compliance, human resources, healthcare and IT areas, offers on-site trainings on a number of areas relating to regulatory compliance.
Boston Scientific stock dropped $1.23 to close at $25.92 yesterday, down 4.5 percent. ... regulatory action without further notice to you,' the agency added. ...
Global New Product Commercialization Product Lifecycle Management Implementing Successful Transformational Change David G. Sherburne Director Global R&D Effectiveness
... time of use; it shall bear an expiration date determined by ... Brown, F. 1993. Review of accidents caused by incomplete inactivation of viruses. Dev. ...
We at Think I are looking for potential business partners in pharmacovigilance and regulatory affairs, Our company is committed to deliver cost effective, flexible , complaint solutions to all pharmacovigilance services (Gap Analysis, Preparing SOPs & WI’ s, PSMF, Imparting PV Training, preparing SDEAs, Integrating QMS PV System, Case processing of ICSR, medical review, MedDRA coding, aggregate reporting, signal detection & risk management)