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medical device manufacturing in continuous improvement program

Operon Strategist is implementing an enhanced continuous Improvement Program (CIP) in response to the feedback that clients have provided to us, about their engagement processes and areas for their performance improvement.<br>Contact details u2013 <br>Phone no - 9325283428<br>Mail - dm@operonstrategist.com<br>Visit - https://www.operonstrategist.com/continuous-improvement-program/?utm_source=ppt and pdf submission&utm_medium=ppt and pdf page&utm_campaign=ppt and pdf submission<br>

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medical device manufacturing in continuous improvement program

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  1. continuous improvement Program consultant | operon strategist Call / Whatsapp - 9325283428 www.operonstrategist.com

  2. Continuous Improvement Program Operon Strategist is implementing an enhanced continuous Improvement Program (CIP) in response to the feedback that clients have provided to us, about their engagement processes and areas for their performance improvement. Continuous Improvement is an ongoing effort to improve products, services or processes Call / Whatsapp - 9325283428 www.operonstrategist.com

  3. Operon Strategist provides below support to the organisations after the certification and licensing activities. ❑ CAPA Monitoring ❑ SOPs Up-gradation as per requirement ❑ Implementation at a site to meet the latest requirements (Eg. 21 CFR) ❑ Customer Complaint Handling ❑ Internal Audit Handling, MRM ( Management Review Meetings) ❑ Need-based Trainings like ISO 9001:2015, ISO 13485:2016 & 21 CFR Part 820 Call / Whatsapp - 9325283428 www.operonstrategist.com

  4. Need-based Training like ISO 9001:2015, ISO 13485:2016 & 21 CFR Part 820 We provide different training courses to help you to understand, implement, and audit to the new version of ISO 9001:2015, ISO 13485:2016, 21 CFR part 820 plus some more in-depth. Call / Whatsapp - 9325283428 www.operonstrategist.com

  5. Training Introductory courses: • Implementation of ISO 9001:2015 This course is all about how to undergo into the new ISO 9001:2015 which is referred to Quality Management Systems. This will help you with the implementation of the changes within your business with specific root cause and corrective action analysis within the organisation. Call / Whatsapp - 9325283428 www.operonstrategist.com

  6. • The requirement of ISO 13485:2016, Medical Device ISO 13485:2016 is the requirement for every medical device manufacturers where they include their management systems in order to gain compliance in the medical device industry. This training will assist you in how to design and develop a medical device as per the international quality standard. And also maintain a quality management system as per internal regulatory standard. Call / Whatsapp - 9325283428 www.operonstrategist.com

  7. •Implementation of 21 CFR Part 820 • Every manufacturer gets knowledge of how to establish and maintain a quality system that is appropriate for their specific medical devices. 21 CFR Part 820 is applicable to any finished medical device for human use, that is manufactured, imported in any State or Territory of the United States. In these courses,cGMP System Regulation is involved that summarizes the essential elements of cGMP regulations governing the methods and facilities used for the servicing, installation, storage, labelling, packaging etc. Finally, the aim of this course is to ensure that finished devices will be safe and effective and otherwise in compliance with the Federal Food, Drug, and Cosmetic Act (the act) Call / Whatsapp - 9325283428 www.operonstrategist.com

  8. Thank You. For More Information Contact Us www.operonstrategist.com info@operonstrategist.com Call / Whatsapp - 9325283428 www.operonstrategist.com

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