Lacidem develos and implements clinical and medical programs for medical device companies with a specific focus on the European markets. New and updated laws and regulations are reinforcing the need for compelling clinical arguments based on safety, efficacy and risk/benefit ratios. Lacidem has the knowledge, expertise and experience to support medical device companies lacking such capacity to be compliant in this new situation.
Whether it is the MEDDEV or the new MDR that was published in 2017, we will ensure that you are compliant. This allows you to do what you do best and always have been doing, namely market and sell your products!