The introduction of a new drug on the market is a very time intensive process taking on average 12 years, going through different milestones requiring different levels of specifications throughout the process.

One of the most challenging steps is the approval by the pharmaceutical authorities of the final drug. This process includes different steps with one involving demonstrating that the drug can be manufactured properly.

To accomplish this task, the manufacturer needs to have suppliers with a high transparency of their supply chain and a strong QA system in place to provide all of the appropriate documentation. CARLO ERBA Reagents is your partner for all of these steps with all the documentation needed for the registration process.

CARLO ERBA Reagents is your partner for chemicals from the R&D all the way to the final production scale. CARLO ERBA Reagents focus on quality ensures that you have a
product that follows all the guidelines needed for the registration of your raw material and/or excipient to the health agencies. CARLO ERBA Reagents QA monitors all the different pharmacopoeias and regulations to assure that your product will always have the right documentation.

To support its pharmaceutical industry partners,
CARLO ERBA Reagents offers two different product lines:
ERBApharm® and XcipharmTM.