Maybe you feel that you have too little in-house expertise on toxicologic pathology. Perhaps your pre-clinical toxicology studies deliver you too many slides. Possibly you are not sure on the quality of the conducted study results. And with everything going on, your sponsor wants you to deliver the results quicker and less expensive. At Global Pathology Support BV we take pride in exceeding our customers’ expectations by making sure that every pathology evaluation and interpretation is conducted with the utmost attention, using the highest international standards (OECD, INHAND Nomenclature, etc.) and Pathology Computer System (Provantis).Many Study Directors feel that multi-site toxicology studies bring extra work and a higher risk of mistakes and misinterpretations. But working harder, correcting other external experts’ work is not a sustainable solution now, is it? In my opinion by outsourcing parts of the process, you’ll save overhead costs while speeding up. Good quality implies that there is enough time for reading slides to prevent damage control in a later stage of the study which is more time consuming. It is inevitable that only an experienced and seasoned toxicologic pathologist is able to perform a profound evaluation which results in sound scientific reports. Being GLP compliant and using the most professional pathology systems and international nomenclatures assures high quality reports.After all: Drugs, chemicals and vaccines should be safe and have no or the least possible side effects. Should you want to discuss how I and/or my company can be of assistance to your pre-clinical research pathology, please do not hesitate to contact me on +31 646149605, via email on bob.thoolen@gpstoxpath.com or send me a direct message.