Freyr Solutions is a leading global Regulatory Solutions and Services company, serving more than 600 companies worldwide in the Life Sciences industry. With its presence in Thailand, Freyr offers end-to-end Regulatory, Labeling, and Clinical services to pharmaceutical, medical device, food, and cosmetic companies. Their expertise lies in areas such as Regulatory Affairs, Regulatory Operations, Labeling, and Market Access. Freyr's dedication to quality and customer satisfaction has earned them a reputation for being a reliable and trusted partner in the industry. Their commitment to innovation and compliance allows companies to navigate the complex regulatory landscape with ease and confidence.

Freyr provides regulatory services and solutions in Sri Lanka to comply with NMRA to pharma, medical device, cosmetics and food supplement manufacturer companies.

Freyr provides regulatory services and solutions in Mexico to comply with COFEPRIS for pharma, medical device, cosmetics and food supplement manufacturer companies.

Freyr provides Regulatory services and solutions in Saudi Arabia to comply with SFDA regulations for pharmaceuticals, medical devices, cosmetics and food supplements manufacturing companies.

Freyr provides regulatory services and solutions in Sri Lanka to comply with NMRA to pharma, medical device, cosmetics and food supplement manufacturer companies.

Freyr is a trusted partner, providing end-to-end Regulatory services, across Top 20 global brands for 6 of the Forbes* Global Top 10 Fortune 500 Healthcare/Life Sciences, Mid-market $1+ Billion Bio Pharma, and Several Small-Medium, Life Sciences Comp

PharmaSolutions International (PSI) provides comprehensive solutions to the pharmaceutical industry, offering services in regulatory affairs, clinical trials, quality assurance, and more. Visit their website at https://www.pharmasolutions-int.com/.

"PharmEng Technology has provided quality services to the Life Science Industry since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products. We provide a wide range of services to the pharmaceutical, biotechnology, medical device, and nutraceutical industries.

Freyr provides End-to-End Regulatory Services in Malaysia to the pharmaceuticals, Medical Device, Food Supplements, and Cosmetic Companies to comply with NPRA Regulations.

MakroCare is a development and Commercialization partner providing consulting, regulatory, clinical, Patient Recruitment, Med Affairs, and Informatics services to Pharmaceutical, Biotechnology and Medical Device industries in USA , Europe & Asia.

Eliquent Life Sciences is a global regulatory consulting firm that helps pharmaceutical, biotech, and medical device companies navigate complex regulatory requirements. Their services include regulatory affairs, pharmacovigilance, quality and compliance, and strategic consulting throughout the product lifecycle. With a team of former regulators and industry experts, Eliquent supports clients worldwide in achieving and maintaining market approval for their products.

QMS Insights' cGMP Consultants specialize in helping pharmaceutical and biotech companies meet regulatory standards for drug and device manufacturing. They offer services like gap analysis, risk assessments, and training to ensure compliance and maintain high-quality production processes.

Di Renzo Regulatory Affairs for over 25 years provides consulting to the major Italian and foreign companies

Freyr provides pharmaceutical regulatory services in Italy for drug & biological product companies which spans across ASMF/CEP, MAA submissions via various procedures (NP, MRP, DCP & CP), dossier preparation, Product life cycle management as p

Freyr provides Cosmetic Regulatory Affairs/Compliance Services for cosmetic industry that span across Product Registration, ingredient review, label and claims review, toxicology assessment and product information file for compliant market entry of product.

Freyr provides regulatory services and solutions in India to comply with CDSCO regulations for pharmaceuticals, medical devices, cosmetics, and food supplements manufacturing companies.

Freyr provides Pharma Regulatory Services in Czech Republic to pharmaceutical manufacturers which spans across MAA Submissions, dossier submissions in eCTD format, QPPV, post-approval support, interaction with HAs as per EU Regulations.

Pharmatech Associates provides consulting and services to the regulated life science industry. Pharmatech’s services cover four spheres of technical expertise that are necessary throughout the complete product development lifecycle: Product and Process Development, Compliance, Regulatory, and Validation.

Pharmadocx provides consultation services to establish Pharma, Cosmetics, Medical Devices & Food Factory and also regulatory services to obtain FDA Drugs License, Cosmetics License, Medical Devices License, FSSAI License. WHO-GMP Certificate, ISO 13485 Certificate.

DDReg Pharma provides comprehensive life science consulting services, specializing in navigating the complex regulatory landscapes of the pharmaceutical and medical device industries. Their expertise spans regulatory strategy, pharmacovigilance, medical writing, and submission management, aimed at accelerating product approvals and ensuring global compliance. DDReg Pharma assists clients throughout the entire product lifecycle, from initial development to post-market surveillance, offering tailored solutions to meet diverse regulatory requirements.

Freyr SUBMIT Pro is one of the best eCTD software tool which helps Life science companies in various regulatory submissions to global health Authorities.

Advamed is a leading medical device regulatory consulting firm that specializes in helping companies navigate the complex world of medical device regulations. With a team of experts who have years of experience in the industry, Advamed provides comprehensive consulting services to ensure that companies meet all necessary regulatory requirements. From FDA submissions to international regulatory compliance, Advamed is dedicated to helping companies bring safe and effective medical devices to market. With a reputation for excellence and a commitment to customer satisfaction, Advamed is a trusted partner for companies looking to succeed in the medical device industry.

MWA shares your commitment to GXP quality and regulatory compliance. As a leader in GXP compliance consulting services, we aim to provide excellence in innovative and holistic solutions to the pharmaceutical, medical device, and biotechnology industries.

TopPharm: Pharmaceutical regulatory affairs and regulatory consulting services in Poland and EU. We offer authorization of medicinal products, medical devices, food supplements, cosmetics, readability testing. We are former authority experts

We provide consultation for Medical and In-vitro Medical Device CE, US FDA, NIOSH, ISO, and Indian MDR certification for various services that meet with regulatory requirements of various countries like UK, USA, India, Europe and more.

Understanding and complying with country registration requirements is essential for successful market entry and ensuring the safety and efficacy of medical devices. Each country may have specific requirements, so it’s essential to consult the respective regulatory authority’s guidelines and possibly seek assistance from regulatory consultants specializing in medical device registration. We at Maven constantly stay updated with the dynamically changing regulations and requirements and keep our clients who have used our services updated with any changes in respective regulations and also send across reminders when their registration are due expiry.

Freyr provides Regulatory Software Solutions to support Global Lifesciences companies that include Pharmaceuticals, Medical devices, Cosmetics and Food Supplement companies to be complaint.

BaiPharm offers the latest pharmaceutical news, in-depth analysis and professional consultancy services. BaiPharm offers a full portfolio of China NMPA compliance consulting services, such as product registration service, registration strategy, GMP compliance service,pharmaceutical & Medical translation service, local agency support and customized training.

A full-service intellectual property and regulatory law firm in Chicago that aids clients to safely navigate the minefield of cosmetic, dietary supplement, drug, medical device and other US food regulations.

RiverArk is a reputable organisation known for its expertise in providing GXP auditing services to pharmaceutical, biotech and medical device companies. With a team of skilled auditors and consultants, RiverArk assists clients in ensuring compliance with regulatory requirements and industry standards. The company's commitment to quality and professionalism has earned them a strong reputation in the industry. Clients trust RiverArk to deliver thorough and comprehensive audits that help them identify and address any compliance issues. With a customer-centric approach and a focus on continuous improvement, RiverArk continues to be a trusted partner for companies looking to maintain the highest standards of quality and compliance.