DR LORNA SPEID, Author at

Tell research subjects the good, the bad and the ugly about entering your clinical trials

That is true informed consent You have worked hard on your clinical trial preparations. Throughout you have had the patient in mind. Have you also taken on board the need for informed consent consulting? The informed consent process is complex with many legal, regulatory and practical considerations. […]

Clinical research consulting paves the way for regulatory approval

The medicines and therapies that make it to market and into the hands of doctors and patients don’t get there by accident. They are the result of careful planning, rigorous testing, and a systematic approach to evaluating safety, effectiveness, and potential risks. Speid & Associates’ Clinical […]

Maximizing Your Probability of Success with Expert Input

Drug Development Consulting Expert drug development can increase the probability of success, because it mitigates risks that you and your team may be unaware of. Drug development programs costs hundreds of millions of Dollars, and so the input that one obtains, and who gives it is […]