The "World Congress on Recycling and Waste Management" is set for August 19-20, 2024, in Paris, France, with a key theme: "Reduce, Reuse, and Recovery for a Better Tomorrow." Centered on Recycling and Waste Management, this global event harmonizes academia and industry efforts toward fostering an eco-friendly environment. Distinguished experts from fields spanning recycling, engineering, and environmental studies converge, facilitating the exchange of insights and pioneering solutions. The Congress aims to propel discussions and innovations, emphasizing a sustainable future through collaborative efforts in Recycling and Waste Management for a greener, more efficient world.

 [Read on recyclingconference.org](https://recyclingconference.org/)

The forthcoming International Conference on Healthcare Quality Management, slated for June 20-21, 2024, in Chisinau, Moldova, is facilitated by a federated organization dedicated to hosting diverse scholarly events within its program. This conference, esteemed for its high quality, offers exceptional value to students, academics, and industry researchers. It endeavors to unite leading academic scientists, scholars, and researchers, fostering the exchange of experiences and research outcomes encompassing Healthcare Quality Management. As a premier interdisciplinary platform, it addresses recent innovations, emerging trends, and practical challenges encountered in this field, encouraging discussions among researchers, practitioners, and educators to advance solutions and insights in Healthcare Quality Management.

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The 2023 Gordon Research Conference on Silk Proteins and the Transition to Biotechnologies will be held in Smithfield, RI. Apply today to reserve your spot. The Silk Proteins and the Transition to Biotechnologies GRC is a premier, international scientific conference focused on advancing the frontiers of science through the presentation of cutting-edge and unpublished research, prioritizing time for discussion after each talk and fostering informal interactions among scientists of all career stages. The conference program includes a diverse range of speakers and discussion leaders from institutions and organizations worldwide, concentrating on the latest developments in the field. The conference is five days long and held in a remote location to increase the sense of camaraderie and create scientific communities, with lasting collaborations and friendships. In addition to premier talks, the conference has designated time for poster sessions from individuals of all career stages, and afternoon free time and communal meals allow for informal networking opportunities with leaders in the field.

Read on:grc.org/silk-proteins

Advanced Technologies & Methods for Global Health & Biodefense June 7-8, 2023 - Eastern Time
 

Reasons to Attend:

- Identify global biological threats and translational gaps in bringing technologies from lab to field.

- Discover infectious disease threats (IDTs) and how different technologies can be applied in diverse operational environments.

- Understand strategic integration for the national strategy for biosurveillance.

- Hear key topics in pathogen detection and technological innovation in ready-to-market systems.

- Meet virtually with speakers and attendees one-on-one and in interactive breakout discussions.

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Dental Conferences: Meet and Join Hands with leading Dental Experts, Dentists and Scientists with their innovative ideas from USA, Europe, Middle East, Asia Pacific, and Africa at Dentists 2023 Conference at Rome, Italy happening on March 20-21, 2023

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Upon completing this program, participants will take home the knowledge to examine their quality management system to determine if it complies with both FDA Quality System requirements and 13485 requirements and recognize where improvements are needed. Participants will learn about the FDA inspectional approach and the Medical Device Single Audit Program. This course will empower the attendee with the knowledge to successfully host an FDA/MDSAP audit.

Upon completing this course, participants will be equipped with the information to able to evaluate the degree of compliance of a design control system, including identification of noncompliance issues, and be prepared to implement the improvements needed to meet requirements.

Upon completing this course, participants will be equipped with the information to able to evaluate the degree of compliance of a design control system, including identification of noncompliance issues, and be prepared to implement the improvements needed to meet requirements.

This 2-day course provides intensive coverage of the elements of a corrective and preventive action (CAPA) system. Some primary topics include the purpose of a CAPA system and how it is integrated throughout a Quality Management System; appropriate data sources and how to coordinate, analyze and manage them; methods for verifying and/or validating actions; how to write good CAPA plans; how risk management is used in conjunction with the CAPA system; and 21 CFR and ISO 13485 requirements.

This intensive 3 – day course provides complete coverage of design control requirements for FDA Quality System Regulation, ANSI/AAMI/ISO 13485:2016, and the Medical Device Single Audit Program (MDSAP). With the participation of FDA representatives during the entire course, attendees have the unique opportunity to participate in a shared learning experience.

This 4.5-day course is the culmination of years of consensus development on the part of a respected group of quality system experts from leading device manufacturers, the FDA, industry consultants, and members of International Organization for Standardization (ISO) standards development teams. Participants will learn how to develop and maintain a quality system program that conforms with the FDA’s Quality System Regulation (21 CFR 820) and ANSI/AAMI/ISO 13485:2016.

This 4.5-day course is the culmination of years of consensus development on the part of a respected group of quality system experts from leading device manufacturers, the FDA, industry consultants, and members of International Organization for Standardization (ISO) standards development teams. Participants will learn how to develop and maintain a quality system program that conforms with the FDA’s Quality System Regulation (21 CFR 820) and ANSI/AAMI/ISO 13485:2016.