Effective Complaint Handling, Medical Device Reporting and Recalls

  • Check with publisher
  • Published date: December 6, 2019
    • Baltimore, Maryland, United States

An effective complaint handling system is an extremely important part of any quality system. Manufacturers should understand that any complaint received on a product shall be evaluated and, if necessary, thoroughly investigated and analyzed, and corrective action shall be taken.

The results of this evaluation should lead to a conclusion regarding whether the complaint was valid, what the root cause of the complaint was, and what action is necessary to prevent further occurrences. Complaints cannot be ignored. They are an excellent indicator of problems with the use, design, and/or manufacture of a product. A single complaint that is thoroughly investigated may lead a company to take remedial or corrective action. It may also take an ongoing analysis of numerous complaints before a trend is spotted that causes a company to initiate changes in their product, labeling, packaging or distribution. The regulatory expectations for both pharmaceuticals and medical devices will be emphasized as well as overview of best practices for timely and effective investigations. Trending is the only way a company can stay on top of emerging quality issues and address those that are most pressing.

Event link: https://www.globalcompliancepanel.com/seminar/-901993SEMINAR?channel=marketplace-mar_2020_SEO
Contact Info:
Netzealous LLC - Globalcompliancepanel
Phone No: 1-800-447-9407
Fax: 302 288 6884
Email: globalcompliancepanel@gmail.com
Website: https://www.globalcompliancepanel.com/

Result 0 votes
John Robinson
0 votes

Useful information

  • Avoid scams by acting locally or paying with PayPal
  • Never pay with Western Union, Moneygram or other anonymous payment services
  • Don't buy or sell outside of your country. Don't accept cashier cheques from outside your country
  • This site is never involved in any transaction, and does not handle payments, shipping, guarantee transactions, provide escrow services, or offer "buyer protection" or "seller certification"

Related listings

  • 6-Hour Virtual Seminar on Tougher Import Rules for FDA Imports in 2020

    6-Hour Virtual Seminar on Tougher Import Rules for FDA Imports in 2020

    Pharmacology - Drug Development Online Event (California) January 17, 2020 Check with publisher

    Importing FDA regulated products requires careful planning before you even start. Registration, product compliance, record and data submission must be exactly correct or your product will be detained. Likewise, the U.S. Customs and Border Protection ...

  • 6-Hour Virtual Seminar on FDA's Software Monsters

    6-Hour Virtual Seminar on FDA's Software Monsters

    Pharmacology - Drug Development Fremont (California) January 17, 2020 Check with publisher

    The complexity and vulnerability of software is expanding exponentially, so fast that Congress removed some device software from FDA’s jurisdiction. The remaining software regulated by FDA presents a degree of a risk to health that creates a public h...

  • 6-Hour Virtual Seminar on Tougher Import Rules for FDA Imports in 2020

    6-Hour Virtual Seminar on Tougher Import Rules for FDA Imports in 2020

    Pharmacology - Drug Development Online Event (California) January 17, 2020 Check with publisher

    Importing FDA regulated products requires careful planning before you even start. Registration, product compliance, record and data submission must be exactly correct or your product will be detained. Likewise, the U.S. Customs and Border Protection ...