IN PARTNERSHIP
Recognition of the work of a CRO: how is it achieved and why?
Find out what a contract research organisation can contribute during the clinical research process. Is its work recognised as often as it deserves, and how does it bring value to your journey?
B
ased in Spain, APICES is a full-service European contract research organisation (CRO) with international
vocation and capabilities, and with more than 13 years of experience. APICES has in-depth knowledge of oncology, immunology, haematology and all other therapeutic areas. It provides a wide range of research and clinical development services, from project design to publication of results, to improve the quality of investigational product development through the optimisation of clinical trials during the development of processes and activities, and the inclusion of non-interventional clinical studies for market access. The goal of APICES is to ensure that you are delighted with our services, providing maximum satisfaction on your clinical development journey. APICES is always striving to exceed client needs and will provide added value by understanding and addressing the main challenges faced by each client during their trials. We will do this through simplifying the clinical development process by implementing key solutions in successful study design, clinical development planning and regulatory timelines to meet our clients’ milestones.
Team drives client satisfaction Always focused on achieving the highest quality results in every project, we tailor our team and resources to the needs and requirements of any study in which we participate. Excellence for our clients and client satisfaction are our key drivers since 2009, proven with >40 public At APICES we have highly trained
professionals, with more than 20 years of
experience in key positions, who have been part of our organisation since its beginnings and provide a real and up-to-date vision of the developments taking place. with extensive experience in CROs and pharmaceuticals. Experts who understand clinical requirements, cultural and linguistic country to implement the best option for a project based on strategic thinking in study design, clinical development planning and successful regulatory strategies.
Experience
partner who can develop and coordinate all the activities which are necessary to carry out clinical research and development. We expertise of our resources, the development of clinical projects of any size and therapeutic area. We provide a full range of services that includes project design, project management, start-up, monitoring, medical monitoring, pharmacovigilance, data management, biostatistics, medical writing and quality assurance, in phases I – IV of clinical trials,
“APICES staff have featured repeatedly in journals in more than 40 acknowledgements”
Outsourcing in Clinical Trials Handbook | 17
Page 1 |
Page 2 |
Page 3 |
Page 4 |
Page 5 |
Page 6 |
Page 7 |
Page 8 |
Page 9 |
Page 10 |
Page 11 |
Page 12 |
Page 13 |
Page 14 |
Page 15 |
Page 16 |
Page 17 |
Page 18 |
Page 19 |
Page 20 |
Page 21 |
Page 22 |
Page 23 |
Page 24 |
Page 25 |
Page 26 |
Page 27 |
Page 28 |
Page 29 |
Page 30 |
Page 31 |
Page 32 |
Page 33 |
Page 34 |
Page 35 |
Page 36 |
Page 37 |
Page 38 |
Page 39 |
Page 40 |
Page 41 |
Page 42 |
Page 43 |
Page 44 |
Page 45 |
Page 46 |
Page 47 |
Page 48 |
Page 49 |
Page 50 |
Page 51 |
Page 52 |
Page 53 |
Page 54 |
Page 55 |
Page 56 |
Page 57 |
Page 58 |
Page 59 |
Page 60 |
Page 61 |
Page 62 |
Page 63 |
Page 64 |
Page 65 |
Page 66 |
Page 67 |
Page 68 |
Page 69 |
Page 70 |
Page 71 |
Page 72 |
Page 73 |
Page 74 |
Page 75 |
Page 76 |
Page 77 |
Page 78 |
Page 79 |
Page 80 |
Page 81 |
Page 82 |
Page 83 |
Page 84 |
Page 85 |
Page 86 |
Page 87 |
Page 88 |
Page 89 |
Page 90 |
Page 91 |
Page 92 |
Page 93 |
Page 94 |
Page 95 |
Page 96 |
Page 97 |
Page 98 |
Page 99 |
Page 100
