ELIQUENT Life Sciences experts Lorna Griffin, Shaun Stapleton, Kathleen Retterson and Julia Carrier, PhD. DABT. will be presenting three insightful sessions at the RAPS Regulatory Strategy Conference on Wednesday, March 12, in Baltimore, USA. Stay ahead of the curve with expert insights from ELIQUENT!??
关于我们
We are expert consultants delivering the answers and solutions that life sciences innovators need to gain and maintain market authorization for their products. Our unprecedented assembly of regulatory leaders, industry experts, and technical specialists collaborate seamlessly to unlock excellence throughout the product lifecycle. We are the convergence of regulatory expertise and technical capabilities across the therapeutic landscape. From thought to finish, concept to commerce, and strategy to execution— ELIQUENT Life Sciences is the singular regulatory resource that clients around the world trust. ELIQUENT Life Sciences is comprised of five global consultancies working as a collective, coordinated regulatory team. The ELIQUENT team includes: VALIDANT: A full-service life science consulting firm providing strategy, execution, and ongoing support for a range of regulatory, compliance, and quality needs. GREENLEAF HEALTH: A leading FDA regulatory consulting firm that provides strategic and technical guidance to pharmaceutical, biotechnology, and medical device companies. DATAREVIVE: A regulatory consultancy firm with expertise to deliver CMC, preclinical, clinical, and GxP expertise to innovators seeking product approvals in major global markets. ORIEL STAT-A-MATRIX: A global leader in training and consulting for business process improvement, regulatory compliance, and quality management systems. IDEC: A regionally specialized regulatory guidance and end-to-end product support for pharmaceutical innovators seeking approval in the Japanese market. Together, ELIQUENT redefines regulatory consulting with a full-service approach and comprehensive solutions that bridge the spectrum of regulatory challenges. Learn more at ELIQUENT.com
- 网站
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https://eliquent.com/
ELIQUENT Life Sciences的外部链接
- 所属行业
- 专业服务
- 规模
- 201-500 人
- 类型
- 私人持股
- 领域
- Regulatory Consulting、Life Sciences、Quality & Compliance、Regulatory Affairs、Pharmacovigilance、Expert Training、Remediation Solutions、Lifecycle Solutions、Global support、Pharmaceuticals、Medical Devices、Combination Products、Biologics、Advance Therapies和Cell & Gene Therpaies
ELIQUENT Life Sciences员工
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Martin Hedley
Executive Transition Coach, Leadership & Governance, Life Sciences
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Julia Carrier, PhD. DABT.
Vice President, Nonclinical Team Lead, ELIQUENT Life Science
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David Husman
Experienced Consultant in Pharmaceutical and Medical Device Industries |Trainer | Based in Greenville |Open to Traveling
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Alistair Macdonald
CEO, Non-Executive Director and Consultant
动态
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ELIQUENT Life Sciences stands with the 300 million people living with a rare disease and is proud to support companies navigating these complexities, ensuring that innovative solutions continue to transform lives. #RareDiseaseDay #ELIQUENTLifeSciences #InnovativeSolutions #RareDiseaseAwareness #TransformingLives
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ELIQUENT Life Sciences is excited to welcome CGT-CMC expert Tiffany Lucas, Ph.D., to our team, bringing her extensive FDA expertise to support innovative therapies and regulatory success! #NewHire #CGT #CellAndGeneTherapy #RegulatoryExpert #LifeSciences #FDAExpert #CMC #Biotech #Innovation #TherapeuticDevelopment
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ELIQUENT Life Sciences is excited to attend the MDMA-FDA Forum on March 12-13 in Palo Alto, CA. Our expert team: Dan Schultz, Heather S. Rosecrans, Mark D. Kramer, Samantha Eakes, MPH will be there. Scan the QR codes below to learn more about our specialists and schedule a meeting.
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Big things happening! ELIQUENT Life Sciences is proud to be a sponsor of the 2025 Regulatory Affairs Professionals Society (RAPS) GRS Conference. Join us as we come together to discuss the latest trends, challenges, and opportunities in the world of regulatory affairs. #RAPS2025 #RegulatoryStrategy #RegulatoryAffairs #LifeSciences
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ELIQUENT Life Sciences is excited to announce the addition of Cell and Gene Therapy Expert, Natika Calhoun! With a proven track record in market authorizations and global inspections, Natika will be a key asset, bringing invaluable expertise to help drive our work forward. Welcome aboard, Natika! #CellAndGeneTherapy #LifeSciences #CGT #RegulatoryAffairs
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The countdown from QSR to QMSR has begun! Stay informed and ahead of the curve with ELIQUENT Life Sciences new MicroLearning sessions – now available on our website: https://lnkd.in/eryPhjpZ #QMSR #FDA #MicroLearning #MedicalDevices
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Stay up to speed with the rapidly changing regulatory landscape. ELIQUENT Life Sciences's new podcast features former #FDA senior officials as they share valuable perspectives and behind-the-scenes insights on the FDA’s transition to a new presidential administration. Hosts Kalah Auchincloss and Brian M. combine real-life experiences with deep institutional knowledge to shed light on how agency transitions impact policies, people, and industry. This podcast is essential listening for anyone in the life sciences industry looking to understand how political shifts shape the regulatory landscape. Listen now at: https://lnkd.in/eq8Z2PRa
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#BIOEurope is a month away. Stop by booth #60 to meet the ELIQUENT Life Sciences team of experts - Helen Barker, Emanuela De Santis (She/Her), Rob McGowan - and learn how ELIQUENT brings clarity to regulatory complexity with a full-service approach and comprehensive solutions that bridge the spectrum of regulatory challenges. Learn more at ELIQUENT.com
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We're excited to announce that ELIQUENT Life Sciences Expert, Katie M. Dale, is leading the EU MDR Auditor Training Course for Europe's Medical Device Regulation (2017/745)! Join her to gain valuable insights and expertise in EU MDR compliance. Learn more about ELIQUENT Life Sciences Expert Training: https://lnkd.in/eHEZMyyd #EUMDR #MedicalDeviceRegulations #EUCompliance #AuditorTraining #ELIQUENTExperts #MedTech
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