RAY CRO is pleased to announce the latest publication of an article entitled ldquo;Level of Agreement and Correlation Between the Estimated Hemoglobin A1c Results Derived by Continuous or Conventional Glucose Monitoring Systems Compared with the Point-of-Care or Laboratory-Based Measurements: An Observational Study rdquo; for the authors Dr. Ayman Al-Hayek Ayman, Dr Samia H. Sobki, Dr Abdulghani H. Al-Saeed, Dr Wael M. Alzahrani and Dr Mohamed A...

RAY CRO is pleased to announce the latest publication of an article entitled ldquo;Level of Agreement and Correlation Between the Estimated Hemoglobin A1c Results Derived by Continuous or Conventional Glucose Monitoring Systems Compared with the Point-of-Care or Laboratory-Based Measurements: An Observational Study rdquo; for the authors Dr. Ayman Al-Hayek Ayman, Dr Samia H. Sobki, Dr Abdulghani H. Al-Saeed, Dr Wael M. Alzahrani and Dr Mohamed A...

Study brief: In light of the current advances in diabetes management, the study aimed to investigate the level of agreement between the standard Lab-HbA1c with point-of-care testing (POCT-HbA1c) and glucose monitoring index (GMI) derived by intermittently scanned CGM (isCGM) or estimated average glucose (eAG) derived by conventional self-monitored blood glucose (SMBG) devices. A cross-sectional study was performed on 81 diabetic patients at Di...

Study brief: For enhanced management of diabetes mellitus, the study authors assessed glucose monitoring satisfaction and clinical efficacy of blood glucose meters featuring color-coded in Type 1 Diabetes patients in Saudi Arabia. The authors included T1DM patients who switched to color-coded Medisafe Fit Smile glucometer. At the end of the study (after 12 weeks), a patient-reported satisfaction with Medisafe Fit Smile color-coded features (MSC...

In 2018, the screening program for the Hepatitis C virus (HCV) was launched as a significant step in the realization of healthcare amelioration in Egypt, orchestrated by President El-Sisi #39;s emphasis on the health and well-being of the Egyptian citizen. Now, the result of this screening program is currently published in one of the prestigious journals in the World (New England Journal Of Medicine).

About the training Course Aims and objectives This training event will familiarize you with the regulatory affairs basic principles, regulations and standards. Participants will learn about the basic skills necessary to work with regulatory agencies (as: WHO, FDA, MOH). It addresses regulatory affairs specialist tasks rsquo; and responsibilities rsquo;. You will know about bio therapeutic products. Who may attend? Do you need basic regulato...

RAY offers consultation in the PV Quality Management Systems (QMS) development, maintenance management RAY has performed more than 50 PV Audits in Africa, Asia and Europe PV audits was launched to develop and improve best practice PV systems and prepare you to the next step of Pharmacovigilance Regulatory Inspections RAY is recognized as regional leading company that provide large client portfolio from small, mid-sized companies to large gl...

RAY proudly announced the launch of 1st locally adapted Automated Literature Review Software InfoDex has a wide database of more than 500 local journals in more than 30 countries in Middle East and Africa RAY can customize your search and automate your review at reasonable prices For more info, Send us your request on Nermin.hassan@ray-cro.com and bd@ray-cro.com

The ICH M7 Guideline on Assessment and Control of DNA Reactive (Mutagenic) Impurities in Pharmaceuticals to Limit Potential Carcinogenic Risk reached Step 4 of the ICH Process in November 2013 and now enters the implementation period (Step 5). The purpose of this new ICH Guideline is to offer guidance on analysis of structure activity relationships (SAR) for genotoxicity. Furthermore, it is intended to resolve questions such as whether impuritie...

At Riyadh Marriott Hotel from Nov 17, 2015 7:30 AM Nov 18, 2015 6:00 PM 2015 Regulatory Science and Best Practices Bringing Innovative Medicines to Patients. http://www.diaglobal.org/en/conference-listing/meetings/2015/11/11th-middle-east-regulatory-conference-merc-2015

The U.S. Food and Drug Administration approved Xuriden (uridine triacetate), the first FDA-approved treatment for patients with hereditary orotic aciduria. Hereditary orotic aciduria is a rare metabolic disorder, which has been reported in approximately 20 patients worldwide. Hereditary orotic aciduria is inherited from a recessive gene. The disease is due to a defective or deficient enzyme, which results in the body being unable to normally s...

RAY aims to provide a forum for international researchers from various areas of pharmacy, medical, Health science and life science by providing a platform for critical analysis of new data, and to share latest cutting-edge research findings and results about all aspects of industrial pharmacy. http://industrialpharmacy.pharmaceuticalconferences.com/

ldquo;Protecting patients, data and reputations rdquo; training held by RAY through an international speaker for a full 3 days; an interactive workshop covers many topics including: Policy decisions for inspectors, Hospitality, FCPA and ABAC; Inspection logistics, Preparation, including dossier request, TMF review, Selecting studies and sites for inspection, Inspecting computerized systems, Conducting interviews, Inspecting monitoring, Inspectin...

ldquo;How to inspect investigator sites and CRO rdquo; was the training held by RAY through international speaker for a full 3 days which started by an introduction to the 3 main agencies EMA, MHRA, FDA were tackling GCP and PV within an interactive workshop context.

The public meeting entitled Information Day on ICH is co-organised by EFPIA and DIA and is intended to provide an update on the status of active topics and potential new topics to be harmonised as well as an update on ICH reforms, including increased transparency, new membership, restructured governance and future funding models. Meeting took place at Vienna, Austria, on March 28th, 2014.

ICH-GCP Training Course for Site Staff Members, training led by our international speaker PhD, MPH.

RAY has received MOH inspection on April 2014, which was conducted by several inspectors covering all aspects from finance to all aspects of ongoing trials; feedback and report came with positive acknowledgment to the effort made by RAY in all aspect of conducting trials and how compliance is strictly respected.

ICH-GCP Training Workshop for Monitors was held through our Consultant GCP Trainer Dr. R. Asaad, BPharm, MSc Pham Med.

Qualification audit was conducted by one of the top 10 global pharmaceutical in KSA, which resulted on contracting RAY with repeated business.