When your pharmaceutical company is working on a new project to develop new medicines, in this scenario, all they need is to take help from the pharmaceutical regulatory consulting company so that the project cannot face any burdens at thi…
If you don’t know, the development process of new drugs is not as easy as it may sound. Most pharmaceutical companies can take between 12 and 15 years from starting to research an active ingredient until it is available to patients. It is …
Today we are going to tell you about the advantages of choosing professional Regulatory affairs services to regularize and host your products. Exporting your products can be a great growth opportunity. The geo-political demand created a fa…
On November 22, 2017, EMA launches a “new and improved” version of EudraVigilance (analogous to FDA Medwatch program). The result will be a total transition in the way that Individual case safety reports (ICSRs) are tracked and reported th…
As professionals in the health area, Medical device consultants have the responsibility to know the health regulation and apply it to comply with it, thus favouring regulatory processes, exercising our profession with responsibility. The U…
Changing lifestyle and eating habits in this current season brings some health challenges as well. Coping with this health disaster is not under the control of every person. Therefore, the invention and research of new medicine is a must t…
Just like any other industry, the pharma industry also contains daily hot topics which could be assigned as the headlines of the present days’ newspapers. By which the updates or the approx.
FDA Drug Labeling is a procedure by which the products and maker companies are investigated sincerely. The product buyers can be able to learn more details from the “full prescribing information” part.
