Brochure
10 Feb 2020
EAS Consulting Group - A Leading Provider of GMP Consulting Services
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EAS Consulting Group
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US
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2015On CPHI since
Other Content from EAS Consulting Group (4)
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Brochure EAS - Services Offered to the Pharmaceutical Industry
EAS provides a variety of FDA based regulatory services to the global Rx and OTC pharmaceutical industry.We offer a seamless approach to help your organization navigate the regulatory intricacies associated with product development, submissions, claims and labeling,manufacturing and packaging of commercial products,as well as facility and product registrations and listings. Our team of pharmaceutical regulatory experts are ready to provide assistance in; the development of filing and quality strategies, GMP/GLP/GCP assessments, Mock-FDA Inspections and reviews, quality management system development, regulatory submissions, product labeling and claims compliance, and a number of other topics that will help your organization succeed in this highly complex and very competitive regulatory environment. EAS is committed to helping the members of domestic and international pharmaceutical market understand,meet and sustain compliance with the FDA’s numerous requirements in a manner t -
Brochure EAS Consulting Group - Your Dedicated U.S. Agent
EAS Consulting Group provides registration and listing assistance as well as US Agent services to international clients in all FDA regulated areas. US Agents are required by FDA to act as an intermediary between foreign firms and FDA. By quickly responding to questions and concerns in a timely manner EAS helps clients get their compliant products to the US marketplace as quickly as possible. -
Brochure EAS Consulting Group - FDA Submission Assistance
The FDA has established a wide variety of product submission requirements across the pharma, device and other regulated segments.Whether you are seeking assistance with an ANDA, DMF, 510(k), GRAS/NDI or a color certification, EAS Consulting Group is a valuable partner in the development and execution of an effective regulatory filing plan to achieve a successful submission. Our team of experts will work with you throughout the product development and submissions life cycle to help you identify the regulatory requirements,assemble product dossiers, evaluate the studies and draft the required submissions documents to give your file the best advantage for successful review by the FDA. We can also assist in maintaining the required facility registrations and product listings as your U.S. Agent -
Brochure EAS Consulting Group Offers Regulatory Support for Food and Drug Law Firms
EAS Consulting Group, LLC is a leading provider of regulatory services to the pharmaceutical, medical device, food, dietary supplement, tobacco, and cosmetic industries. Whether your firm is looking for an expert witness in litigation involving FDA requirements, policies,and procedures; remediation, warning letters and 483 responses, or assistance with the preparation and submission of regulatory documents, audits and investigations, EAS senior consultants with both FDA and high-level industry experience can provide valuable assistance.
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