b'2.CentralizedScheduling.Ourintegratedoperations,sites,and scheduling system allow us to accelerate your timeline, ensuring we avoid potential roadblocks before they materialize.3.Parallel Processing. We run certain processes in parallel, and overlap activities to ensure that your program is streamlined and efficient from the get-go. Our regulatory, scientific, and operational experts are an integral part of the process planning, actively managing your timeline to make sure your project stays on track, always moving forward.4.Dedicated Project Management. Sounds like a lot of moving parts, you say? It is, and our dedicated, cross-functional Program Managers willhandlethemallforyou.Whetheritbescientific,operational, administrative, or other, your Program Manager will stay with every aspect of your program, for its entire duration. 5.Communication.Clear,consistent,constantcommunicationtiesall these offerings togetherbetween services, departments within those services, with third parties, regulatory agencies, and finally, with you, our clients. Whether an end-to-end program or a single study, you only have to Tell Us Once, and well take care of the rest. We make sure that everyone involved understands your preferences, your requirements, your past and present projects, and the future plan. Transparent and proactive communication is critical to the efficient completion of your roadmap to success.The combined impact of all these innovative approaches is something we call Proactive Drug Development. Its where we bring all our expertise, passion, knowledge, and innovation to bear so that your program has the greatest chance of success. Our company is structured so that we have two Co-Chief Operating Officers who ensure that all the services and sites are fully integrated, harmonized, and collaborating, to deliver the best value for you.Choosing the right CRO/CDMO partner makes all the difference. For a single study or a full program (or something in between), Altasciences is your drug development partner of choice.'