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Preclinical Safety

What You Need To Know Planning for an IND Submission

What You Need To Know Planning for an IND Submission

For drug developers ready to progress a molecule to the pivotal clinical trial stage, filing an Investigational New Drug (IND) application with the U.S. Food and Drug Administration (FDA) is a significant milestone. Drug developers approach this task with a wide range...

Virtual Audits: You Can Now Qualify Testing Sites From Home

Virtual Audits: You Can Now Qualify Testing Sites From Home

Between travel limits and social distancing, in-person visits at testing sites for drug and medical device development are currently not an option. Qualifying testing sites is a standard industry practice, but the resulting restrictions of COVID-19 present new...

Keeping Your Molecule’s Timeline on Track During COVID-19

Keeping Your Molecule’s Timeline on Track During COVID-19

The unforeseen and drastic effects the COVID-19 pandemic has had on the industry have led to unanticipated challenges, including stricter international shipping regulations, travel restrictions, local lockdowns and more. However, industry leaders are still here to...

Through Partnership We Will Push Forward

Through Partnership We Will Push Forward

As your partner we are taking all the necessary steps to make sure your drug development continues without any disruptions in the process. Moving your molecule forward during COVID-19 doesn’t need to be stressful or difficult. We continue to learn and have found...