SYNCORP Clincare Technologies (P) Ltd.

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SYNCORP Clincare Technologies (P) Ltd. India Office: Corporate Office: Novel Business Centre No.

Bangalore - 560 068 (INDIA) Tel: 91-080-65474772 / 91-080-50072226 E-mail: info@syncorp.in Visit us at: www.syncorp.in and www.

301, 3rd Floor, Vijetha Classic Empire, Beside ICICI Bank, Chaithanyapuri, Dilsukhnagar, Hyderabad - 500060, INDIA

1 SYNCORP Clincare Technologies (P) Ltd. India Office: Corporate Office: Novel Business Centre No. 10, 100 Feet Ring Road, BTM Layout 1st Stage. Bangalore (INDIA) Tel: / info@syncorp.in Visit us at: and Regional Office: Telangana - Hyderabad Branch: No.301, 3rd Floor, Vijetha Classic Empire, Beside ICICI Bank, Chaithanyapuri, Dilsukhnagar, Hyderabad , INDIA Tel: / / Odisha - Bhubaneswar branch: Syncorp Business Center Plot No. F29 (Near Aroma Institute) P.O. BJB Nagar (Behind BJB College) Bhubaneswar (Odisha), INDIA Tel: / /

2 About Syncorp SYNCORP Clincare technologies (P) Ltd. ( was established in the year 2010 and we are serve Pharma/Biotech companies, CROs, KPO/ BPOs with wide range of best clinical consul ng and service solu ons. Syncorp is fastest growing organiza on has it s presence at Bangalore as a Head Quarter and have other clinical business units in Hyderabad and Bhubaneswar in India. SYNCORP educa onal trust ( is associated with the University of Mysore offers Master Degree in Clinical Research, other Diploma Course, PG Graduate Programs and Professional skill development programs. Our Vision A leading consul ng and contract research organiza on driven by knowledge, integrity and performance commi ed to our clients success. Our Mission Our purpose is to enable our customer businesses to manage their services tailored to meet the specific and ever-changing business challenges. Build shareholder value by delivering pharmaceu cal and healthcare products, services and solu ons in innova ve and cost effec ve ways by consistently enabling businesses to produce superior opera ng results. Syncorp s USP 1. Our team and consultants have decade plus year of experience in Clinical consul ng and services sector. 2. Strong Clinical Trial sites management capability to support global trials in India, including eastern part of India. 3. Strong team with Interna onal and Indian Regulatory experience in wri ng regulatory documents for USFDA, EMA and DCGI submissions. 4. Exper se in academic scien fic wri ng. 5. Team s exper se in clinical research, discovery and pre - clinical research, diagnos cs and other health care services. 6. Manpower consul ng/ Resource management system in place to assist our customer in their talent acquisi on strategy we have large diverse profiles database. 7. Our learning and development academy affiliated to University of Mysore. 8. Large pool of Industry experts in our teaching academy. 9. Customized Learning Management system, to support the con nuous skill development of the staff and individuals Main Goal: Syncorp Clincare Technologies (P) Ltd., established in 2010 has emerged as one of the fastest growing service provider in life sciences and healthcare sector. It provides services in Manpower Consul ng, CRO/SMO Services, Educa on/ Training & Clinical Solu ons. Our Goal is serve our clients and emerge as one of the leaders in life sciences and healthcare sector.

3 Syncorp Clincare Service Offerings Snapshot Service Line Manpower Consul ng CRO/SMO Services Educa on/ Training Clinical Solu ons Data Services Sta s cal services CROs/ BPOs/ Diagnos cs/ Health care Fresher Lateral Hiring Leadership Hiring Clinical trial site management Clinical Trial Monitoring Staff Trainings Corporate trainings- GCP/ GLP/ ISO Quality Training Pursuit Management-RFP/ RFI consul ng CRO/ SMOs- Business Process Reengineering Quality Management Consul ng Services - CRO/ SMO/ Pharma/ cgmp GLP/ Diagnos cs management PMS study Management Publica on Support Marke ng Materials prepara on, Product monograph, Visual Aid, Slides for Healthcare Professional Product Development materials including graphics designing Training for sales force Academics & Healthcare Professionals Diploma M.Sc. Programs (Affiliated to University of Mysore) - course for Pharma/ Life Science/ Medical science/ graduate/ Post Graduate Manuscript wri ng Abstract wri ng/ Case report wri ng Con nuous Medical Educa on content Prepara on Thesis wri ng support Sta s cal analysis Resume/ Profiles Development Website Designing- Healthcare professionals Syncorp Clincare Service Offerings Manpower Consul ng: We offer services as a consultancy in various ways such as assis ng the companies to hire from leadership roles to freshers. We provide customized solu on to our customer to support their manpower/ talent acquisi on strategy requirements, and we work closely to fulfill the need by ac vely finding the right skilled individuals from job market and individual references.

4 CRO/SMO Services: We offer a wide range of CRO ac vi es related to clinical trials including, Regulatory submission, Project Management, Monitoring & other SMO services for different therapeu c domains. Educa on and Training: We offer Diploma courses designed for Life Science/ Pharma science/ Medical science graduates and Postgraduates on key domains of clinical research such as CR, CDM, PV, Clinical SAS, Medical Wri ng and Regulatory Affairs to fulfill the needs of the pharmaceu cal industry. We offer M.Sc. (Clinical Research) full- me course that is recognised by University of Mysore to educate and train students in depth about ethical and scien fic perspec ves of clinical research. Also, we offer corporate training at different levels to keep abreast with the updates and train professionals in GCP, GMP, GLP, Data Services, Quality, Professional skill development training. Clinical Solu ons: Our strength lies in providing clinical consul ng solu ons for business setups such as CROs/ BPOs/ pharmaceu cal & Biotech organisa ons in Life-science and healthcare. Our services include : i) End to end Deal pursuit Management (RFP/ RFI management/ Process reengineering of CRO/ SMO business processes); ii) Clinical data Management, sta s cal analysis; iii) Quality management (QA); SOP wri ng, Qualifica on audits ISO, GLP, NABL, CAP & other regulatory audits; iv) Setup & maintenance of GLP accredited laboratory facility; v) Medical & scien fic Wri ng: a) Academic Scien fic Wri ng: Supporting academicians and healthcare professionals in publica on ac vi es (manuscript, abstract, case study etc); Slide prepara on for con nuous medical educa on and doctor s conference. b) Commercial-CRO s/ Pharma Scien fic Wri ng: Medico-Marke ng Materials: Content development and designing of promo onal materials like product monograph, presenta on slides and visual aids etc; Sales force training manual and training of the sales force; Regulatory Wri ng: Investigator s Brochure, Protocol, Clinical Study Report, Case Report Forms for Post Marke ng Surveillance Studies (PMS); Sta s cal Support- Bio- sta s cal Data Analysis and Sta s cal Analysis Plan and Report Genera ons.

5 Service Profile Case Studies Project Management monitoring, clinical consul ng solu ons for CROs for clinical trial including complying with update and train professionals ; irement, GLP and Regulatory requgcp in GCP, GMP, GLP, Data Services and Quality. Global CRO that is part of US based Organiza on, in business since It was founded in 2006, is a privately clinical consul ng solu ons for business setups such as CROs/BPOs/pharmaceu cal organisa ons owned pharmaceu cal services company with its business offices in Los Angeles, CA and Bangalore, India. It has some of industry s top management and scien fic talent, along with state of the art R & D facility in Bangalore, India Randomized, Double Blind, Placebo Controlled, Phase III Study to assess the Safety and Efficacy. Dura on of the study is 2 years with 48 pa ents approved by US FDA. Site Management ac vi es closed on me with good Quality. Customized, Well governed Project plan & execu on to correspondence with CRO, Coordina on between CRO and Inves gator, Collect and maintain regulatory documents from inves ga ve sites, Organize and prepare trial related materials and presenta ons for Inves gator mee ngs. Ethi cs Commi ee submission, Site set up and document collec on, Prepare site for SIV, Provide dedicated trained study coordinator to clinical trial site for site works, Independent site monitoring for quality check of trial documents. (ii) Good turnaround me in site management & closure ac vi es Well coordinated site management - without any major escala ons On me Coordina on between site and CRO for trial-related ac vi es including Ethics Commi ee submission. Service Profile Corporate training at different levels to keep abreast with the updates and train professionals in GCP, GMP, GLP, Data Services, Quality, Professional skill development training. Global CRO (It provides high quality, appropriately priced solu ons and services with global scalability to life sciences clients addressing their cri cal business and scien fic needs. It is designed to deliver high quality and cost effec ve solu ons and services for our clients in the Americas, Europe, Asia, La n America and Australia.) 67 candidates to be trained in GLP within 15days. Qualify staff in GLP Prac ces to support regulatory audit. Customized Training solu on & execu on. Staff assessment with GLP cer fied consultant Par cipa on cer ficate issued to support the audit. As agreed delivered the customised trainings in 15 days of me and supported the customer regulatory audit.

6 (iii) Service Profile Provide customized solu on to our customer to support their manpower/ Talent Acquisi on strategy requirements. Global CRO (Established and privately held since It is a leading CRO with mul na onal presence in 40 Countries.) (iv) 10 Plus leadership posi ons (Sta s cal/sas Programmers Skill mappings done for all leadership roles iden fied and Biosta s cians) to be closed within 45 days to support Mapped the role within Syncorp database immediate ramp up strategy of our client. Target hiring the candidates & short listed the required number Support customer to roll out offer to candidate and engage with candidate ll they onboard. Supported our customer ramp up plan and met client requirement within the scheduled meframe. Service Profile Project Management services for clinical trials - Monitoring and site management. Pharma Company (It is fully integrated company, known around the globe for its research and development ini a ves and breakthroughs. It is supported by world class manufacturing facili es accredited with na onal and interna onal cer fica ons, state -of -the -art research centre, rich Intellectual Property Wealth, a strong marke ng network worldwide coupled with dedicated and highly efficient professionals.) Trial Randomized, Parallel Group, Ac ve Controlled, Open label study to determine the safety and efficacy (2 Trials) Dura on of the study is 1.6 years with 147 pa ents approved by DCGI Project Management ac vi es closed on me with good Quality. Customized, Well governed Project plan & execution to Correspondence with Sponsor, Independent site monitoring for quality check of trial documents, Routine site monitoring, Study close - out visit Collect and maintain regulatory documents from investigative sites, Organi ze and prepare trial related materials and presentations for Investigator meetings. Ethics Committee submission, Site set up and document collection, Prepare site for SIV, Provide dedicated trained study coordinator to clinical trial site for site works, Independent site monitoring for quality check of trial documents. Good turnaround me in site management & closure ac vi es. Well coordinated site management - without any major escala ons. On me Coordina on between site and Sponsor for trial -related ac vi es including Ethics Commi ee submission. Our Presence: We offer our services in 3 prominent loca ons Bangalore, Hyderabad, & Bhubaneswar in India.

OUR MISSION. Working Together. Delivering Solu ons. Improving Lives

OUR MISSION. Working Together. Delivering Solu ons. Improving Lives ANNUAL REPORT 2016 OUR MISSION Working Together In partnership with our established network of 3,000 partner organiza ons, we design and manage programs to operate seamlessly. Delivering Solu ons Customized,