Maintaining Your Supplier Controls During the COVID-19
Every year Medpoint consultants conduct hundreds of supplier
audits around the globe for our medical device, pharmaceutical, and biotech clients. These audits are conducted by our certified auditors, generally on-site at supplier locations, to evaluate compliance with quality management system standards and regulations. However, in these times of the COVID-19 pandemic, we have been helping our clients by pivoting to remote auditing. We are very experienced in conducting these audits remotely using various conferencing technologies. Maintaining the periodic, critical evaluation of your suppliers and their quality management systems is an essential aspect of controlling the inputs to your supply chain.
Medpoint has highly credentialed, experienced, and certified auditors around the globe. Our auditors have language capabilities to effectively conduct audits in most countries and can execute audits without travel and without the person-to-person exposure risks associated with on-site, face-to-face audits. We have exceptional auditors that can conduct
audits against Quality Management System standards and regulations including, but not limited to, the following:
- 21 CFR 820
- 21 CFR 210/211
- 21 CFR 600
- ISO 9001
- ISO 13485
- ISO 17025
- ISO 14971
- EU Regulations
Medpoint, an ISO 9001:2015 certified company, provides distinctive recruiting and consulting services in the areas of quality assurance, regulatory, and clinical affairs for our global medical device, pharmaceutical, and biotech client
companies. You can depend on our technical expertise, availability, and competitive rates.
Let us help you to maintain your supply chain compliance – we can help you with all of your supplier quality and auditing needs.
Contact us today: firstname.lastname@example.org or 844-MEDPOINT (844-633-7646)