Expert Training fromcomplextoclear
Expert Training
ELIQUENT experts provide in-person and remote training services to empower both leadership teams and employees with the skills and tools to create pragmatic problem-solving processes and maintain adherence to evolving regulatory, compliance, and quality standards. Our training solutions equips internal teams to drive continual improvement and help build a common culture of accountability.
ELIQUENT redefines regulatory consulting with a full-service approach and comprehensive solutions that bridge the spectrum of regulatory challenges. Our integrated suite of solutions aligns with your goals to unlock regulatory success.
Strategic & Technical Capabilities
ELIQUENT’s highly specialized experts provide both strategic direction and hands-on execution services that guide clients from the earliest phases of development through post-market support.
In-Person, Virtual & On-Demand
Training for teams, private groups, and individuals.
Regulatory Policies & Procedures
Expert instruction on all aspects of regulatory programs across the product lifecycle.
Quality Systems
Foundational and in-depth learning programs on quality management systems across the regulatory landscape.
Inspectional Readiness
Specialized programs to ensure readiness prior to regulatory inspections.
Customized Training Programs
Flexible options to develop training programs on a variety of regulatory subjects.
Unmatched Expertise
Our unprecedented assembly of regulatory leaders, industry experts, and technical specialists set the standard for regulatory consulting excellence. With decades of experience in senior positions at the FDA, EMA, and throughout industry, ELIQUENT’s team of respected professionals brings unmatched expertise that companies need when working directly with the regulators and when navigating today’s evolving regulatory environment.
Focus Areas
ELIQUENT’s foundation is built on experts with the foremost strategic and technical skill across markets, pathways, and global regulations. ELIQUENT’s specialized solutions showcase our collective capabilities and combined expertise. Together, we create a full-service model that equips clients with a premier regulatory resource.
Market Solutions
With a robust understanding of global regulatory requirements, ELIQUENT provides tailored solutions that support pharmaceutical, biotechnology, medical device, and combination product companies navigating the complex regulatory landscape. Our team of highly qualified experts bring decades of regulatory, quality, safety, and clinical experience in the following markets specialties:
Drugs & Biological Products
ELIQUENT’s team of experts provide strategic and technical guidance on drugs and biologics from product development to regulatory review and beyond post-market requirements.
Advanced Therapies & CGTs
Our team of regulatory and clinical experts apply their specialized skill set to move complex therapies through the regulatory process to manufacturing and beyond.
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Areas of Expertise:
Monoclonal Antibodies
Enzyme Replacement Therapies
Biosimilars
Tissue-Based Therapies
Vaccines
Combination Products
Unlock the full potential of your combination product. Our team supports companies developing combination products with expert guidance throughout the product lifecycle.
Devices & Diagnostics
Leverage our team’s extensive experience as you navigate the process of bringing new devices and diagnostics to market and manufacturing them to quality standards.
Industry Due Diligence
ELIQUENT applies vast institutional knowledge to equip investors with the information needed to ensure life science transactions account for business objectives, regulatory risks, and the industry landscape.
Cosmetics
ELIQUENT’s knowledge and understanding of the evolving cosmetics regulatory landscape provides clients with a trusted partner when developing and commercializing cosmetic products in compliance with regulations.
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Areas of Expertise:
Product labeling & claims
MoCRA Requirements
Compliance service offerings
Regulatory policy solutions
Expert training
Learn more about ELIQUENT’s Cosmetics Solutions:
INFO SHEET: Cosmetics Regulatory Solutions >>
Find a Training Course
ELIQUENT provides world-class training courses designed to equip professionals in the life sciences industry with the knowledge and skills they need to navigate complex regulatory, quality, and compliance challenges. With decades of experience, we are a trusted partner for companies seeking to improve their operations, ensure regulatory compliance, and enhance product quality.
Our comprehensive training programs cover a wide range of critical topics, from FDA and ISO regulations to risk management, CAPA, auditing, and beyond. Whether you’re a seasoned professional or just starting your career, our expert-led courses provide practical, real-world solutions to help you excel in today’s competitive regulatory environment.
Global Solutions
Expertise beyond borders. ELIQUENT’S established and growing global presence spans the regulatory process and major markets. Our premier team of global regulatory experts support markets across the U.S., Europe, and Asia.
United States
ELIQUENT is a leading Food & Drug Administration (FDA) regulatory consulting firm that provides strategic and technical guidance to pharmaceutical, biotechnology, and medical device companies.
Our experts have shaped the landscape of FDA regulatory policy and strategy for decades. We bring this unrivaled knowledge and unique insight to our work with clients every day.
Europe
The ELIQUENT team applies their deep and diverse knowledge of European regulations to keep clients in lock step with evolving global standards. With decades of experience in the European market, our team understands the intricacies of the European Medicines Agency (EMA) and offers tailored solutions to ensure products meet and exceed the needs of our clients.
Asia
ELIQUENT offers regionally specialized solutions for the innovators across Asia. Our comprehensive solutions include expert guidance to innovators seeking approval in Japan, the third-largest pharmaceutical market in the world. Explore ELIQUENT’s solutions for clients in Japan’s life sciences market.
Explore ELIQUENT Japan >>
Integrated Solutions.
Full-Service Support
ELIQUENT’s unprecedented assembly of regulatory leaders, industry experts, and technical specialists collaborate seamlessly to provide a full-service engagement that delivers end-to-end support. No matter your pathway position, regulatory requirements, global market, or therapeutic area – ELIQUENT’s integrated solutions align with your regulatory goals to unlock regulatory success.
Regulatory Affairs Solutions
PV+ Post Market Surveillance
Quality & Compliance
Remediation Solutions
Talent Solutions
From the earliest phases of innovation through regulatory submissions, to post- approval support, our robust blend of technical skill and clinical expertise guide companies to approval and beyond.
With an approach that includes both strategic direction and hands-on global support, ELIQUENT’s customized pharmacovigilance solutions empower companies to operate with confidence.
Our team of highly specialized quality & compliance experts build customized solutions that equip companies with best-in-class strategic support, technical expertise, and project-based solutions.
ELIQUENT’s Remediation Solutions address challenges head-on, providing the expert guidance life science innovators need to bring your operations back into compliance and securing your path forward.
Whether you need a team of one or 100+, ELIQUENT’s talent solutions gives you the ability to rapidly scale your team to the right size, with the right level of expertise, in the right locations.
Your resource for regulatory clarity.
IQ Central is your resource for industry insights, expert perspectives, and valuable tools. Here, you’ll find a comprehensive collection of collateral, expert resources, and thought leadership designed to support your goals and keep you informed on the latest trends and help you navigate today’s regulatory landscape.
Resources
THOUGHT LEADERSHIP
Impact of R&D Quality Systems & Data Integrity in Drug Development
Read Steven Bowen, Ph.D.’s article in the Journal of Pharmaceutical Sciences.
Read more
Case Study: Global Regulatory Solutions
Learn how ELIQUENT Japan guided a global immunology company to regulatory success.
Read moreSOLUTIONS
Regulatory Writing
Explore ELIQUENT’s Regulatory & Medical Writing Solutions.
Regulatory Writing Solutions
IQ Central
ELIQUENT Outcomes: Global Medical Device Firm Acquisition
IQ Central
ELIQUENT Outcomes: Japan Biopharmaceutical Indication
IQ Central
ELIQUENT Outcomes: Private Equity Diligence of Multiple Excipient Manufacturing
IQ Central