Brochure
10 Feb 2020
EAS Consulting Group - FDA Submission Assistance
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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 - A Leading Provider of GMP Consulting Services
EAS provides a variety of domestic and international regulatory services to industries under FDA oversight including in-depth expertise and guidance in the areas of Good Manufacturing Practices (GMPs), Good Laboratory Practices (GLPs),Good Clinical Practices (GCPs), and Good Documentation Practices (GDPs) for all FDA regulated industries. EAS conducts compliance assessments and mock FDA inspections for manufacturers, packagers, distributors, Own Label Distributors, contract manufacturers, laboratories, Research& Development facilities, Contract Research Organizations and more. Our seamless approach helps organizations navigate the many regulatory requirements for compliance with quality management and system development. Whether your firm is involved with the manufacturing, packaging,distribution of products; ingredients and additives; or is a testing or research laboratory facility; EAS is committed to helping you understand, meet and sustain compliance with the FDA’s numerous -
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 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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