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The Old Barrel Store Draymans Lane Marlow, Buckinghamshire, SL7 2FF United KingdomG&L utilizes decades of experience and a wealth of Subject Matter Expertise in Regulatory Affairs, Quality Assurance and Clinical Development to design and deliver solutions to the biggest challenges faced by global healthcare today. G&L’s reputation for designing and delivering highly effective solutions to the biggest challenges in global healthcare and our commitment to ensuring that our clients’ specific requirements are always met have seen the company experience phenomenal growth since our establishment in 2016. From product development and submissions to company-wide change management, G&L Healthcare Advisors is proud to design, implement, and maintain high-quality, results-focused outcomes for everyone with whom we work. As regulatory experts across the entire product lifecycle, we assist in early development, filing strategy, pre- and post-approval CMC, MAA/NDA support, publishing, post-approval lifecycle management (LCM), and global projects. Whether you require specific technical skills, short or long-term temporary workload support, or a comprehensive project team, we would love to discuss your needs further. On the Quality Assurance side - from clinical to commercial, our expertise will help you guarantee compliance, maintain oversight and eradicate risk, allowing you and your team to focus on your core deliverables. We provide: • QMS development and gap analysis • Clinical trial audits and site inspection preparation • Vendor management support • Inspection readiness, including inspection support • API and DP audits • Remediation support • eTMF gap analysis and audits • Clinical trial material and commercial product release
Lanyon Tower, Lanyon Plaza, 7 Lanyon Place, Belfast, Antrim, BT13BT IrelandG&L utilizes decades of experience and a wealth of Subject Matter Expertise in Regulatory Affairs, Quality Assurance and Clinical Development to design and deliver solutions to the biggest challenges faced by global healthcare today. G&L’s reputation for designing and delivering highly effective solutions to the biggest challenges in global healthcare and our commitment to ensuring that our clients’ specific requirements are always met have seen the company experience phenomenal growth since our establishment in 2016. From product development and submissions to company-wide change management, G&L Healthcare Advisors is proud to design, implement, and maintain high-quality, results-focused outcomes for everyone with whom we work. As regulatory experts across the entire product lifecycle, we assist in early development, filing strategy, pre- and post-approval CMC, MAA/NDA support, publishing, post-approval lifecycle management (LCM), and global projects. Whether you require specific technical skills, short or long-term temporary workload support, or a comprehensive project team, we would love to discuss your needs further. On the Quality Assurance side - from clinical to commercial, our expertise will help you guarantee compliance, maintain oversight and eradicate risk, allowing you and your team to focus on your core deliverables. We provide: • QMS development and gap analysis • Clinical trial audits and site inspection preparation • Vendor management support • Inspection readiness, including inspection support • API and DP audits • Remediation support • eTMF gap analysis and audits • Clinical trial material and commercial product release
25 Independence Boulevard Warren, NJ, 07059 United StatesG&L utilizes decades of experience and a wealth of Subject Matter Expertise in Regulatory Affairs, Quality Assurance and Clinical Development to design and deliver solutions to the biggest challenges faced by global healthcare today. G&L’s reputation for designing and delivering highly effective solutions to the biggest challenges in global healthcare and our commitment to ensuring that our clients’ specific requirements are always met have seen the company experience phenomenal growth since our establishment in 2016. From product development and submissions to company-wide change management, G&L Healthcare Advisors is proud to design, implement, and maintain high-quality, results-focused outcomes for everyone with whom we work. As regulatory experts across the entire product lifecycle, we assist in early development, filing strategy, pre- and post-approval CMC, MAA/NDA support, publishing, post-approval lifecycle management (LCM), and global projects. Whether you require specific technical skills, short or long-term temporary workload support, or a comprehensive project team, we would love to discuss your needs further. On the Quality Assurance side - from clinical to commercial, our expertise will help you guarantee compliance, maintain oversight and eradicate risk, allowing you and your team to focus on your core deliverables. We provide: • QMS development and gap analysis • Clinical trial audits and site inspection preparation • Vendor management support • Inspection readiness, including inspection support • API and DP audits • Remediation support • eTMF gap analysis and audits • Clinical trial material and commercial product release
25 Independence Boulevard Millburn, NJ, 07059 United StatesG&L utilizes decades of experience and a wealth of Subject Matter Expertise in Regulatory Affairs, Quality Assurance and Clinical Development to design and deliver solutions to the biggest challenges faced by global healthcare today. G&L’s reputation for designing and delivering highly effective solutions to the biggest challenges in global healthcare and our commitment to ensuring that our clients’ specific requirements are always met have seen the company experience phenomenal growth since our establishment in 2016. From product development and submissions to company-wide change management, G&L Healthcare Advisors is proud to design, implement, and maintain high-quality, results-focused outcomes for everyone with whom we work. As regulatory experts across the entire product lifecycle, we assist in early development, filing strategy, pre- and post-approval CMC, MAA/NDA support, publishing, post-approval lifecycle management (LCM), and global projects. Whether you require specific technical skills, short or long-term temporary workload support, or a comprehensive project team, we would love to discuss your needs further. On the Quality Assurance side - from clinical to commercial, our expertise will help you guarantee compliance, maintain oversight and eradicate risk, allowing you and your team to focus on your core deliverables. We provide: • QMS development and gap analysis • Clinical trial audits and site inspection preparation • Vendor management support • Inspection readiness, including inspection support • API and DP audits • Remediation support • eTMF gap analysis and audits • Clinical trial material and commercial product release
Seven Giralda Farms Suite 120 Madison, NJ, 07940 United StatesG&L utilizes decades of experience and a wealth of Subject Matter Expertise in Regulatory Affairs, Quality Assurance and Clinical Development to design and deliver solutions to the biggest challenges faced by global healthcare today. G&L’s reputation for designing and delivering highly effective solutions to the biggest challenges in global healthcare and our commitment to ensuring that our clients’ specific requirements are always met have seen the company experience phenomenal growth since our establishment in 2016. From product development and submissions to company-wide change management, G&L Healthcare Advisors is proud to design, implement, and maintain high-quality, results-focused outcomes for everyone with whom we work. As regulatory experts across the entire product lifecycle, we assist in early development, filing strategy, pre- and post-approval CMC, MAA/NDA support, publishing, post-approval lifecycle management (LCM), and global projects. Whether you require specific technical skills, short or long-term temporary workload support, or a comprehensive project team, we would love to discuss your needs further. On the Quality Assurance side - from clinical to commercial, our expertise will help you guarantee compliance, maintain oversight and eradicate risk, allowing you and your team to focus on your core deliverables. We provide: • QMS development and gap analysis • Clinical trial audits and site inspection preparation • Vendor management support • Inspection readiness, including inspection support • API and DP audits • Remediation support • eTMF gap analysis and audits • Clinical trial material and commercial product release
Seven Giralda Farms Suite 120 Madison, New Jersey, 07940 United StatesG&L utilizes decades of experience and a wealth of Subject Matter Expertise in Regulatory Affairs, Quality Assurance and Clinical Development to design and deliver solutions to the biggest challenges faced by global healthcare today. G&L’s reputation for designing and delivering highly effective solutions to the biggest challenges in global healthcare and our commitment to ensuring that our clients’ specific requirements are always met have seen the company experience phenomenal growth since our establishment in 2016. From product development and submissions to company-wide change management, G&L Healthcare Advisors is proud to design, implement, and maintain high-quality, results-focused outcomes for everyone with whom we work. As regulatory experts across the entire product lifecycle, we assist in early development, filing strategy, pre- and post-approval CMC, MAA/NDA support, publishing, post-approval lifecycle management (LCM), and global projects. Whether you require specific technical skills, short or long-term temporary workload support, or a comprehensive project team, we would love to discuss your needs further. On the Quality Assurance side - from clinical to commercial, our expertise will help you guarantee compliance, maintain oversight and eradicate risk, allowing you and your team to focus on your core deliverables. We provide: • QMS development and gap analysis • Clinical trial audits and site inspection preparation • Vendor management support • Inspection readiness, including inspection support • API and DP audits • Remediation support • eTMF gap analysis and audits • Clinical trial material and commercial product release
25 Independence Boulevard Millburn, New Jersey, 07059 United StatesG&L utilizes decades of experience and a wealth of Subject Matter Expertise in Regulatory Affairs, Quality Assurance and Clinical Development to design and deliver solutions to the biggest challenges faced by global healthcare today. G&L’s reputation for designing and delivering highly effective solutions to the biggest challenges in global healthcare and our commitment to ensuring that our clients’ specific requirements are always met have seen the company experience phenomenal growth since our establishment in 2016. From product development and submissions to company-wide change management, G&L Healthcare Advisors is proud to design, implement, and maintain high-quality, results-focused outcomes for everyone with whom we work. As regulatory experts across the entire product lifecycle, we assist in early development, filing strategy, pre- and post-approval CMC, MAA/NDA support, publishing, post-approval lifecycle management (LCM), and global projects. Whether you require specific technical skills, short or long-term temporary workload support, or a comprehensive project team, we would love to discuss your needs further. On the Quality Assurance side - from clinical to commercial, our expertise will help you guarantee compliance, maintain oversight and eradicate risk, allowing you and your team to focus on your core deliverables. We provide: • QMS development and gap analysis • Clinical trial audits and site inspection preparation • Vendor management support • Inspection readiness, including inspection support • API and DP audits • Remediation support • eTMF gap analysis and audits • Clinical trial material and commercial product release
25 Independence Boulevard Warren, New Jersey, 07059 United StatesG&L utilizes decades of experience and a wealth of Subject Matter Expertise in Regulatory Affairs, Quality Assurance and Clinical Development to design and deliver solutions to the biggest challenges faced by global healthcare today. G&L’s reputation for designing and delivering highly effective solutions to the biggest challenges in global healthcare and our commitment to ensuring that our clients’ specific requirements are always met have seen the company experience phenomenal growth since our establishment in 2016. From product development and submissions to company-wide change management, G&L Healthcare Advisors is proud to design, implement, and maintain high-quality, results-focused outcomes for everyone with whom we work. As regulatory experts across the entire product lifecycle, we assist in early development, filing strategy, pre- and post-approval CMC, MAA/NDA support, publishing, post-approval lifecycle management (LCM), and global projects. Whether you require specific technical skills, short or long-term temporary workload support, or a comprehensive project team, we would love to discuss your needs further. On the Quality Assurance side - from clinical to commercial, our expertise will help you guarantee compliance, maintain oversight and eradicate risk, allowing you and your team to focus on your core deliverables. We provide: • QMS development and gap analysis • Clinical trial audits and site inspection preparation • Vendor management support • Inspection readiness, including inspection support • API and DP audits • Remediation support • eTMF gap analysis and audits • Clinical trial material and commercial product release
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The Contract Research Map is owned and maintained by Scientist.com. It was created to help researchers in the life sciences identify and connect with contract research organizations (CROs) based on geography. Updated nightly, this map features all of the available CROs within our network, so you can order services with a few clicks. Click on a specific country, scroll on the map itself or type into the search bar at the top—there are many ways to find the location and suppliers that you’re looking for. From Argentina to New Zealand, use this map to connect with a CRO near you.
We believe that every researcher across the world should be able to connect with the thousands of global CROs that exist and have the opportunity to work together. Like many industries,the life science supply chain has been disrupted over the last year. But there are many other circumstances such as international customs regulations or sensitive shipping times that create limitations around which countries are feasible to partner with. Sometimes, finding a CRO based in a country that best suits your research needs is imperative. We hope this contract research map allows you to find the right partner in the right place at the right time.
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