Introduction: Welcome to dicentra! We are a diverse team from a wide range of industries and backgrounds all united by one common passion: to improve the health and wellness of […] Read More >>
Introduction: Welcome to dicentra! We are a diverse team from a wide range of industries and backgrounds all united by one common passion: to improve the health and wellness of […] Read More >>
On July 20, 2022, Health Canada published amendments to the Food and Drug Regulations (FDR), introducing new regulations for supplemented foods as a category. These new regulations continue to protect […] Read More >>
New labelling requirements announced by Health Canada in Canada Gazette, Part II, Volume 156, Number 14 titled “Regulations Amending the Natural Health Products Regulations” have come into effect as of […] Read More >>
Introduction: dicentra is seeking a passionate and people-oriented Recruiter to lead the growth of our team. At dicentra, our people are our most important asset; as the Recruiter, your role […] Read More >>
The cost to obtain an MDEL (Medical Device Establishment Licence) and MDL (Medical Device Licence) in Canada depends on the medical device’s classification. In this blog, we will break down […] Read More >>
Introduction: dicentra is seeking an experienced and detail-oriented Clinical Research Coordinator/Phlebotomist to join our growing team. The Clinical Research Coordinator/Phlebotomist will conduct clinical trials with study participants in accordance with Read More >>
Introduction: We are looking for a “go-to” person for all employee-related issues to join our team as a Human Resources (HR) Coordinator. The ideal candidate will be developing and implementing […] Read More >>
Bioanalysis is the quantitative evaluation of analytes/substances in biological matrices such as tissue, blood, serum, urine, or other body fluids. Bioanalytical testing involves using a validated bioanalytical method for the […] Read More >>
The following factors will drive the global regulatory affairs outsourcing market growth during the forecast period: Increasing Use of Digital Platforms/Solutions in Regulatory Affairs.Changing Regulatory Landscape.Rising Demand For Fast Drug […] Read More >>
Introduction: The Principal Investigator (PI) is primarily responsible for assuring clinical trial research is conducted in compliance with the laws, regulations, disciplinary standards, and ethics guidelines relevant to clinical research […] Read More >>
Leading contract research organization and professional consulting firm dicentra is proud to announce that their valued client, NNB Nutrition, has successfully achieved self-affirmed GRAS (Generally Recognized as Safe) status for […] Read More >>
This blog is meant to be an overview of the average costs associated with bringing a medical device to market under normal circumstances. Depending on when you are reading this […] Read More >>
Introduction: We are looking for an experienced and assertive senior-level Clinical Research Associate/Clinical Study Monitor who would be responsible for the overall monitoring of clinical trials, ensure compliance with the […] Read More >>
Introduction: The Quality Assurance Associate (Importation) will be mainly responsible for overseeing the importation of Natural Health Products, preparation of Product Master Files/Quality Summary Reports and NNHPD FPS as well […] Read More >>
The new European Union In Vitro Diagnostics Regulations (EU IVDR) entered into application on May 26, 2022, to replace In Vitro Diagnostic Medical Devices Directive (98/79/EC). Manufacturers, authorized representatives, importers, and […] Read More >>
Introduction: Reporting to the CEO with a dotted line to the Principal Investigator (PI), the Director of Clinical Research Operations performs a key leadership role within the organization. The Director […] Read More >>
In vitro diagnostic medical devices contain a broad spectrum of devices that test biological samples to determine the status of one’s health, from self-tests for pregnancy, to blood glucose tests […] Read More >>
EFSA’s Strategy 2027 delineates the European Food Safety Authority (EFSA) strategies and approaches in responding to the changing environment in the years ahead, especially in light of the SARS-CoV-2 global […] Read More >>
Carbiotix (publ) (“Carbiotix” or “Company”) announces today a confirmed timeline for the completion of GRAS Self Affirmation (SA) and the date that the Company’s CarbiAXOS nutraceutical ingredient will be launched in [&he Read More >>