Websites using clinical trial reporting as a keyword

Zuellig Pharma is Asia's leading healthcare services provider offering a broad range of innovative services including distribution of pharmaceuticals, medical devices and clinical trial materials, sales and marketing outsourcing, patient-centered programs, payor services (third party administration services), clinical reach, patient care, channel, consumer health, animal health, insurance and a full range of retail pharmacy services.

Tri County Sleep Medicine offers sleep consultations and treatment for people with sleeping disorders in the St. Louis, Missouri and surrounding areas.

Ayush 82: Ayush 82 CCRAS, CCRAS, Central council for research in ayurvedic sciences, Ayush 82 NRDC, National research development corporation

International Conference on Harmonisation of technical requirements for registration of pharmaceuticals for human use. A standard for the design, conduct, performance, monitoring, auditing, recording, analyses, and reporting of clinical trials that provides assurance that the data and reported results are credible and accurate, and that the rights, integrity, and confidentiality of trial subjects are protected. Ethical and scientific quality standards for designing, conducting, recording and reporting trials that involve participation of human subjects to ensure that the RIGHTS, SAFETY and WELLBEING of the trial subjects are protected. Ensure the CREDIBILITY of clinical trial data. ICH GCP (E6): TABLE OF CONTENTS

Expert translation and review in 150 languages and dialects. Uniquely qualified to serve medical device, clinical trial and test publishing companies.

Rely on Quorum Review IRB for unsurpassed customer service, high performance independent review board services and 24 hour turnarounds.

Laboratory Mission Control: Sampleminded manages mission critical specimens and test results for regulated diagnostics labs, research labs and clinical trials.

Electronic data capture for today's clinical research. Randomize subjects, collect patient-reported outcomes and manage trial site data with one platform.

がん情報サイト「オンコロ」は、オンコロジー（腫瘍学）をテーマにして、最良のがん医療に繋がる研究、治験や臨床試験、がんに関する様々な診療・治療情報などを配信するがん情報ポータルサイトです。がん患者やご家族だけでなく、オンコロジストを始めとする医療者にとっても、有益ながん情報を配信していきます。

safety data managementclinical data management3d avatar3d anatomical modelsafety data visualizationsignal detectionadverse eventsclinical data reviewclinical trial data managementelectronic medical recordselectronic healthcare recordspersonalized healthcare recordspatient information systemshospital information systemsvisual health | Data Integration and Information Management for Health and Life Science Data.

株式会社クロエは、被験者募集をメインとしたCRO（Contract Research Organization/医薬品開発業務受託機関）事業に医家向け広告代理店機能を加えた国内初のPRO(Patient　Recruitment Organization/被験者募集機関)です。治験に関わるフィージビリティスタディからサイトセレクション、被験者リクルートメント、フォローアップまでワンストップで支援いたします。

Best-in-class global clinical trial payment technology.

ClinicalTrialFacts.com provides information on over 100,000 clinical research studies & trials. Our goal is to be the most widely visited, comprehensive, and informative site about current and past research.

PHASTAR is a specialist CRO offering statistical consultancy, clinical trial reporting and data management services by providing expert consultants and delivering in-house projects. Our number one priority is to ensure that the work we produce is of the highest quality: every project PHASTAR undertakes is supervised on methodology and utilises internal processes designed to ensure optimal quality. Services include production of clinical study reports including generating tables, figures and listings; study design and protocol writing; modelling and simulation; and advice on handling missing data across phase I to IV trials. Our headquarters is in Chiswick, London (UK) with additional offices across four continents. We partner with pharmaceutical and biotech companies globally..

Leaders in digital patient engagement and data capture (ePRO and eCOA) solutions for clinical trial and digital health programs

Quality Data Services, Inc. is a full service contract research organization specializing in You - Your data, Your clinical trial, Your results.

Mental health clinical trials research center in Jackson MS investigates medications to find better treatments for mental disorders, bipolar, ADHD, alzheimer,

SaaS Precision Medicine applications and tools for data analytics research and workflow needs in Life Science, Health IT, Biospecimens, Clinical Trial, Pharmaceuticals

clinical trial enrollment services, including clinical trial patient recruitment, study feasibility, patient retention, patient surveys and site selection

QBECO SSI is a new investigational treatment for ulcerative colitis and Crohn's disease designed to restore the body’s innate immune system and correct the dysfunctional immune response related to inflammatory bowel disease. QBECO SSI is being studied in clinical trials for IBD.

治験･健康食品･ｺｽﾒﾓﾆﾀｰなどお得情報いっぱいの生活向上ﾓﾊﾞｲﾙ

Laboratory Mission Control: Sampleminded manages mission critical specimens and test results for regulated diagnostics labs, research labs and clinical trials.

治験・臨床試験の最新情報を日本中のサイトから集めた情報キュレーションサイト、治験情報ネット。実施エリア毎に入院・通院タイプのモニター・ボランティア情報を掲載。男性・女性、健康な方・病気の方全ての募集を網羅。治験をアルバイトと伝えているようなあやしいサイトからは情報抽出はしていませんので、ご安心してお使いください。

ABO VYTAL® | Fysiek en Mentaal herstel bij Burn-out of PTSS

IDDI provideS the best in class trial design, clinical data collection, standardization, analysis and reporting to your clinical trials.

View the official health care professionals website with clinical trial information and resources on NovoLog®.

Clinical Trial Management and Medical Scheduling Software

Jyton Group is one of the first companies offering consulting and information services for medical device and pharmaceutical products in the world. primary service covers medical device china,IVD Approval in china,CFDA registration,IVD Approval in china and so on.

The only patient-centric supply chain organization in the life sciences industry.

EDC, ePRO, eCRF, CTMS, CDMS, electronic data capture, clinical trial and PMS software