亚洲精品成人免费_91女神娇喘疯狂3p之夜_精品韩国一级久久_av毛片网_www超碰com_午夜视频体内射.COM.COM

印度Siro-Clinpharm 
Siro-Clinpharm印度CRO企業
SIRO Clinpharm 榮獲 Frost & Sullivan 2012年度最佳臨床研究組織印度醫療保健獎，致力于為全球醫療保健行業提供藥品開發解決方案。

該公司的學科專業知識讓其在臨床數據管理、醫學寫作、生物統計、臨床試驗管理和臨床試驗供應等領域擁有一定的優勢。其治療業務范圍包括但不限于腫瘤學、糖尿病、心臟病學、傳染病和呼吸道疾病。該公司提供靈活的業務模式，按照客戶需求提供全方位立體化服務。

Vision

We will be a leading drug development solutions provider by delivering compelling value propositions to the global healthcare industry.

Mission

We will provide exceptional drug development solutions through our passion for excellence and unwavering commitment.

To achieve our mission, we will

? Deliver the advantages of non-traditional geographies through our expertise and customer oriented approach.
? Provide a nurturing work culture that stimulates professional excellence through training.
? Empowerment with accountability and recognition.
? Provide a fair return on investment to our investors by driving aggressive growth and efficiency.
? Enable delivery of new medicines, while maintaining the highest ethical standards and be a responsible corporate citizen.
 SIRO is a full- service clinical research organization with experience in all phases of clinical trials and in all key areas of the drug development process. You can count on SIRO to support all aspects of your clinical development plans in India.


Clinical Trials
From an Idea to an approved product, a drug's journey through the complex development process is often anxiety -filled. The most critical component in this process is clinical development. It is very critical for a company to make sure that the identified opportunity has the best chances for success. Clinical trials account for the largest component of the cost and the timelines, and also the greatest risk for things to go wrong. Each phase has its own set of challenges and you need a partner that has seen it all and is capable of meeting your needs from phase I to IV.



At SIRO, it is our endeavor to make sure that all studies receive a high level of attention to detail, the same quality of clinical services and regulatory compliance. To ensure this we offer you our experienced project managers and multifunctional study teams.

The teams work closely with investigators, patients, and sites and are backed by tools and processes that are designed to avoid the many pitfalls that often plague clinical trials. Our teams are trained to ensure that all protocols are followed and deadlines met.

Our proactive and creative approach to ensure the acceleration of the clinical trial is what keeps our clients satisfied with our services and ensures a high level of repeat business.

We invite you to explore our services that can be sourced invidually or as a part of a full scope study.

Feasibility and patient access planning
Project Management and Planning
Clinical Monitoring
Medical Services
Clinical Audit Services and Quality Assurance

Other related services that can be sourced individually

Site contract management
Clinical resourcing
Investigator recruitment
CRF design
Clinical data management
Biostatistics
Medical Writing