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Regulatory Affairs Press Releases

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By Lorax Compliance Ltd
Lorax Compliance Complimentary Webinar. This Webinar will give you a clearer understanding of how to forecast, and minimize the budgetary impact of EPR compliance on your sustainability goals
By Pentland Brands
Pentland, owner of some of the world’s most high-profile and popular sports, outdoor and fashion brands, has outsourced its packaging data management to Lorax Compliance, a global expert that helps companies meet their legal obligations.
12402475
By Spectrum Regulatory Solutions
Spectrum Regulatory Solutions, a company that provides a full-service consultancy to the healthcare industry, boosts its regulatory team by appointing Natasha Long as a Regulatory Project Manager.
12386625
By Spectrum Regulatory Solutions
Spectrum Regulatory Solutions, a company that provides a full-service consultancy to the healthcare industry, continues its expansion by appointing Karen Cornelius as Regulatory Project Manager for Medical Devices.
By FDAnews
9th Annual FDA Inspections Summit **Presented by FDAnews** Oct. 22-24, 2014 – Bethesda, MD www.fdanews.com/InspectionsSummitPR1
By marcus evans
Marcus evans Legal Series invites Senior In-House Counsel and Heads of FATCA, Regulatory Compliance, and Tax Operations from Leading Financial Institutions to Share Best Practices for Preparing for the Future of Global Tax Compliance
By Q1 Productions
Regulatory Approvals in China, 510(k) Guidance Among This Years’ Discussion Topics
By Q1 Productions
Investigator-Led Research, Timeline and Resource Management Among Session Topics at Inaugural Event
By Q1 Productions
Helping Regulatory Affairs Executives around the World Remain Current on Evolving Regulatory Guidance within the Device & Diagnostic Industries, from Securing Regulatory Approval to Meeting Post-Market Vigilance Requirements
By SFL Regulatory Affairs & Scientific Communication
SFL experts will present on EU medical device/IVD law, public & regulatory affairs synergies and transparency of payments to the healthcare sector
By SFL Regulatory Affairs & Scientific Communication
SFL’s Managing Director, Shayesteh Fürst-Ladani will be giving presentations at two upcoming Swiss life science events on revision of EU Medtech legislation.
By SFL Regulatory Affairs & Scientific Communication
SFL’s Managing Director provides regulatory insight into Drug Device Combination Products in Europe.
By Compliance Trainings
Scheduled On : Thursday, July 18, 2013 at 1:00 PM EDT Duration : 60 Minutes
By MakroCare
MakroCare, an international Drug Development and Commercialization services firm will be exhibiting at DIA-2013, Boston, Massachusetts.
12154436
By SFL Regulatory Affairs & Scientific Communication
SFL to attend the DIA 49th Annual Meeting (Booth 1744) in Boston June 23-27, 2013.
12146354
By SFL Regulatory Affairs & Scientific Communication
Shayesteh Fürst-Ladani will speak at the Market Access Preliminary Skills for Regulatory Professionals event.
By SFL Regulatory Affairs & Scientific Communication
SFL is pleased to announce the constitution of its company Advisory Board.
12092035
By SFL Regulatory Affairs & Scientific Communication
SFL's Managing Director invited to speak at biotech workshop in Germany
12088357
By SFL Regulatory Affairs & Scientific Communication
SFL team showcase expertise in Regulatory Affairs, Public Affairs, Legal Services and Medical Communications at the 2013 DIA Annual EuroMeeting in Amsterdam.
By SFL Regulatory Affairs & Scientific Communication
Shayesteh Fürst-Ladani, SFL’s Managing Director, will give a presentation on the classification and regulation of drug/device combinations at the MEDTEC Europe event to be held in Stuttgart, Germany from 26 to 28 February 2013.

All Press Releases

By Q1 Productions
International Guidelines, FDA Meeting Preparation Strategies Among New Discussion Topics
By Lorax Compliance Ltd
Lorax Compliance Complimentary Webinar. This Webinar will give you a clearer understanding of how to forecast, and minimize the budgetary impact of EPR compliance on your sustainability goals
By Pentland Brands
Pentland, owner of some of the world’s most high-profile and popular sports, outdoor and fashion brands, has outsourced its packaging data management to Lorax Compliance, a global expert that helps companies meet their legal obligations.
By Lorax Compliance Ltd
Michelle Carvell, director of client services at Lorax Compliance, explains the legislation behind the EPR directives.
By Freyr Solutions
In a collaborative initiative Freyr co-authored the first joint white paper with Beroe Consulting addressing the Global Regulatory Trends, Challenges and Solutions faced by Global Pharma Industry in the Consumer Healthcare space.
By Compliance Global Inc
This webinar will outline fundamental components of adiversion prevention, detection, and response program. An overview of the scope of the problem will be provided, and safety and quality implications will be demonstrated.
By Compliance Global Inc
This webinar will outline fundamental components of adiversion prevention, detection, and response program. An overview of the scope of the problem will be provided, and safety and quality implications will be demonstrated.
By Spectrum Regulatory Solutions
Spectrum Regulatory Solutions, an innovative healthcare consultancy, has launched a new website to mark its tenth year in business.
By Q1 Productions
New UDI Regulations, Global Labeling Requirements Among Discussion Topics at Second Semi-Annual Meeting
By Reagan-Udall Foundation for the FDA
Extension of grant from the Bill & Melinda Gates Foundation to facilitate community engagement in TB drug development; education for regulatory scientists
12402475
By Spectrum Regulatory Solutions
Spectrum Regulatory Solutions, a company that provides a full-service consultancy to the healthcare industry, boosts its regulatory team by appointing Natasha Long as a Regulatory Project Manager.
By Q1 Productions
Represented Presenting Organizations to Include FDA, USDA, U.S. Customs and Border Protection
12386625
By Spectrum Regulatory Solutions
Spectrum Regulatory Solutions, a company that provides a full-service consultancy to the healthcare industry, continues its expansion by appointing Karen Cornelius as Regulatory Project Manager for Medical Devices.
By FDAnews
9th Annual FDA Inspections Summit **Presented by FDAnews** Oct. 22-24, 2014 – Bethesda, MD www.fdanews.com/InspectionsSummitPR1
By marcus evans
Marcus evans Legal Series invites Senior In-House Counsel and Heads of FATCA, Regulatory Compliance, and Tax Operations from Leading Financial Institutions to Share Best Practices for Preparing for the Future of Global Tax Compliance
By Q1 Productions
Regulatory Approvals in China, 510(k) Guidance Among This Years’ Discussion Topics
By Spectrum Regulatory Solutions
Spectrum Regulatory Solutions, a company that provides a full-service consultancy to the healthcare industry, appoints two new medical writers to further expand its busy team, headed up by Dr Simon Thorn, Scientific Affairs Director.
By ELC Group
Inna Demidova to head new Moscow office for fast-growing global regulatory affairs specialist
By Q1 Productions
Investigator-Led Research, Timeline and Resource Management Among Session Topics at Inaugural Event
By Q1 Productions
Social Media Implications, Solidifying Data for On-Site Presentation Among Key Topics
By IBRI NOIDA
DMF, Dossier, CTD, eCTD, Clinical Regulatory Affairs, Quality Assurance and Control
By Q1 Productions
Helping Regulatory Affairs Executives around the World Remain Current on Evolving Regulatory Guidance within the Device & Diagnostic Industries, from Securing Regulatory Approval to Meeting Post-Market Vigilance Requirements
By GlobalSubmit
Software Release Includes New Module 1 Specifications, Performance Enhancements
By SFL Regulatory Affairs & Scientific Communication
SFL experts will present on EU medical device/IVD law, public & regulatory affairs synergies and transparency of payments to the healthcare sector
By SFL Regulatory Affairs & Scientific Communication
SFL’s Managing Director, Shayesteh Fürst-Ladani will be giving presentations at two upcoming Swiss life science events on revision of EU Medtech legislation.
By SFL Regulatory Affairs & Scientific Communication
SFL’s Managing Director provides regulatory insight into Drug Device Combination Products in Europe.
By ELC Group
World-renowned clinical scientist John Warren joins ELC GROUP’s Advisory Board
By MakroCare
MakroCare expands CPC (Clinical Processing Center), it offers centralized, regional or local clinical processing services to biopharmaceutical and device companies.
By Environmental Systems
Why hire expensive full time technical employees when part time contract employees can complete the necessary tasks and keep your company in compliance with federal and state laws.
By MakroCare
MakroCare today announced the addition of Vistaar, a Regulatory Intelligence tool, to it's RA portfolio. Reg Intel was always the foundation of MakroCare services, with Vistaar, it’s formalized as a tool that it’s customers can benefit from.

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