Toxicology Program Design Management

Regulatory and Technical Associates, Inc. (RTA) is a consulting company that specializes in a wide range of toxicology program design and management consulting activities. Our consultants are Board Certified in Toxicology, Regulatory Affairs and Safety and have years of experience in toxicology program design, clinical research, and regulatory affairs. We work with clients both internationally and domestically, and provide superior design and management consulting services to our clients.

Our consultants have extensive experience in toxicology program design, management, consulting, implementation, conduct, data interpretation, monitoring and reporting of preclinical testing programs. Regardless of whether your testing calls for a single study or an entire testing program to support your regulatory submission, RTA has the experience to address your needs working with an approved Contract Research Organization (CRO) or your own in-house testing facility.

RTA has extensive experience with toxicology program studies of all types, some of which include safety pharmacology, toxicokinetics, local tolerance (irritation and sensitization), phototoxicity, acute toxicity, repeat dose toxicity, in vitro and in vivo genotoxicity, reproduction/developmental toxicity and carcinogenicity. RTA also has experience conducting programs to evaluate the toxicity of unique metabolites, product degradants and impurities.  Our program design and management professionals are experienced with all large and small laboratory species and with all routes of administration.

We routinely assist our clients with any and all phases of study and toxicology program conduct including, but not limited to, bid preparation, protocol development, CRO selection, study implementation, GLP compliance, and dosing confirmation analysis. In addition, RTA is able to provide experienced toxicology program consulting services to support your in-house testing activities.  We are also able to provide extensive report writing and regulatory submission services.

RTA has the necessary experience in toxicology program design to help our clients address the product development issues that directly impact their ability to bring their products to market.

For more information regarding how we can assist you with your toxicology program design and management consulting activities please contact Dr. Robert J. Staab (phone: 860-434-5872;  email: rta1ali1@aol.com) or Dr. Ira Daly (phone: 908-236-6834; email: idaly61127@aol.com).