Aclairo has broad experience calculating F factors across numerous drug classes and indications.
Author Archives: admin
Aclairo Welcomes New Staff
Aclairo is pleased to welcome Emilia Kostadinova to our team as Contracts Administrator. She is excited to move into contracts after many years working in litigation. She will be responsible for the negotiation and maintenance of the company’s consulting agreements and all related confidentiality agreements. Emilia can be contacted at (703) 506-6760 ext. 309 or ekostadinova@aclairo.com.
Happy Holidays!
The Aclairo offices will be closed for the holidays from December 24th through January 2nd. Senior consultants will be available via email to address any urgent matters.
Holiday Closure
The Aclairo office will be closed Thursday the 24th and Friday the 25th for the Thanksgiving holiday.
New Services for eCTDs
Aclairo has purchased eCTD software which allows us to maintain your regulatory submissions in eCTD format for the product’s lifecycle. Clients can access their submission remotely at any time, making that final review before submitting to the FDA that much easier! For more information on our new service, please contact Dana Dunn at ddunn@aclairo.com.
Aclairo Welcomes a New Consultant
We’re excited to announce a new addition to the Aclairo team, Dr. Dana T. Minnick. She will be working as a consultant specializing in preclinical drug development. Welcome Dana!
Join Aclairo at ACT 2011
Dr. Sheevers and Dr. Guttendorf will be speaking at the 32nd Annual Meeting of the American College of Toxicology, November 6th – 9th at the Arizona Biltmore Resort & Spa. We look forward to seeing you there! For information on the event and registration, visit www.actox.org.
Dr. Hilary Sheevers
CE Class Title: Opportunities During Change: Advancing Your Toxicology Career in an Uncertain Market
Date: Sunday, November 6, 2011 (1:00 – 4:30 PM)
Talk: Transitioning From an 8-5 Job to Consulting (3:00 PM)
Symposium II: Update on Preclinical Oncology Drug Development
Date: Monday, November 7, 2011 (9:00 AM – 12:00 PM)
Talk: Introduction to the Toxicology Side of Oncology Drug Development
Dr. Robert Guttendorf
CE Class Title: Non-Clinical ADME in Safety Assessment
Date: Sunday, November 6, 2011 (8:00 – 11:30 AM)
Talk: Absorption and Pharmacokinetics (8:00 AM)
Aclairo’s New Online Presence
Welcome to our brand new company website! We have re-designed and re-organized the Aclairo website to give it a user-friendly and modern layout. Check out the services pages to discover how Aclairo can facilitate your drug development program and contact us today!