CrushSCI.com
Journal Selection & Manuscript Polishing Services
Therapeutic Innovation & Regulatory Science journal cover Medicine
Back to journal directory

Review Cycle Records

Therapeutic Innovation & Regulatory Science

Springer SCIE Non-OA
2026 Emerging Zone 42025 CAS Zone 42025 JCR Q3
167.7Average days
158Median days
44Fastest days
303Longest days
1682025 publications

Paper Review Records

All Paper Review Records

15 valid samples · Newest publication first
Review days = acceptance date − received date. PDF, DOI, and publisher-page sources are retained.

158 days

Validation of the Ontario Protocol Assessment Level (OPAL) Tool for Assessing Clinical Trial Complexity and Supporting Workforce Planning in the Italian Clinical Research Context

AuthorsDaniele Napolitano; Mattia Bozzetti; Rosario Caruso; Monica Guberti; Ileana Frau; Bobbi Smuck; Gionata Fiorino; Franco Scaldaferri; Lucrezia Laterza; Antonio Gasbarrini; Vincenzina Mora

Affiliations1. Scientific Direction – Fondazione Policlinico Universitario IRCCS, Università Cattolica del Sacro Cuore Rome, Rome, Italy; 2. Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy; 3. Direction of Health Professions, ASST Cremona, Cremona, Italy; 4. Department of Biomedical Sciences for Health, University of Milan, Milan, Italy; 5. Health Professions Research and Evidence Transfer Unit, IRCCS MultiMedica, Sesto San Giovanni, Italy; 6. Nursing and Allied Health Professions, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy; 7. Ass. Prime Site Director, Strategic Site Solutions EMEA - IQVIA, Milan, Italy; 8. Department of Ophthalmology, Ivey Eye Institute, St. Joseph’s Health Care, London, Canada; 9. Gastroenterology and Digestive Endoscopy, San Camillo-Forlanini Hospital, Rome, Italy; 10. Centro Malattie dell’Apparato Digerente (CEMAD), Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Università Cattolica del Sacro Cuore, Rome, Italy

Source PDF DOI Publisher page
210 days

Implementing Project Optimus in Oncology Dosage Optimization: Where are We Now?

AuthorsRevathi Ananthakrishnan; Patrick Mitchell; Dong Xi; Gu Mi; Gina D’Angelo; Haijun Ma; Yujun Wu; Philip He

Affiliations1. Bristol-Myers Squibb (BMS), Princeton, USA; 2. AstraZeneca (AZ), Gaithersburg, USA; 3. Gilead, Foster City, USA; 4. Sanofi, Cambridge, USA; 5. Revolution Medicines, Redwood City, USA; 6. Oncolytics Biotech Inc, San Diego, USA; 7. Daiichi Sankyo, Inc, Basking Ridge, USA

Source PDF DOI Publisher page
182 days

The Effect of Covariate Adjustment for Cox Regression in Cardiovascular Outcome Trials

AuthorsAlexander Przybylski; Björn Holzhauer; Simon Wandel

Affiliations1. Novartis Pharmaceuticals UK Ltd., London, UK; 2. Novartis Pharma AG, Basel, Switzerland

Source PDF DOI Publisher page
303 days

Current Status and Construction Requirements of Drug Clinical Trial Institutions in Sichuan Province in China

AuthorsShuxia Shi; Shangyuan Qin; Qin Yu

Affiliations1. National Drug Clinical Trial Institution of West China Second University Hospital, Sichuan University, Chengdu, China; 2. NMPA Key Laboratory for Technical Research on Drug Products In Vitro and In Vivo Correlation, Chengdu, China; 3. Children’s Medicine Key Laboratory of Sichuan Province, Chengdu, China; 4. Key Laboratory of Birth Defects and Related Diseases of Women and Children, Sichuan University, Ministry of Education, Chengdu, China; 5. Department of Pharmacy, Chengdu Fifth People’s Hospital, Chengdu, China

Source PDF DOI Publisher page
112 days

The CARE Program: An Initiative of Patient-Focused Drug Development for Rare Diseases by NMPA

AuthorsLing Tang; Songmei Xie; Lijia Yuan; Xiaowen Xu; Xing Ai; Tian Zhao; Zhimin Yang

Affiliations1. Center for Drug Evaluation, National Medical Products Administration, Beijing, The People’s Republic of China

Source PDF DOI Publisher page
286 days

Utilization of Clinical Evaluation Reports in Japan’s Medical Device Approvals: Insights from Review Data on Approved Devices

AuthorsKoji Yamada; Daisuke Obata; Jun Matsubayashi; Mayumi Yamanaka; Akiko Hinomura; Hiromu Kutsumi; Shin-ya Morita; Shu Kasama

Affiliations1. Center for Clinical Research and Advanced Medicine, Shiga University of Medical Science, Seta Tsukinowa-cho, Otsu, Japan; 2. Asahi Kasei Medical Co., Ltd., Tokyo, Japan; 3. Clinical & Translational Research Center, Kobe University Hospital, Kobe, Japan; 4. Medical Research Support Center, University of Fukui Hospital, Eiheiji-cho, Yoshida-gun, Fukui, Japan; 5. Department of Pharmacotherapeutics, Shiga University of Medical Science, Seta Tsukinowa-cho, Otsu, Japan

Source PDF DOI Publisher page
156 days

Measuring Centralized Patient Outreach Recruitment Strategies and their Costs in Clinical Trials

AuthorsJennifer Y. Kim; Mary Jo Lamberti; Hana Do

Affiliations1. Tufts Center for the Study of Drug Development (CSDD), Tufts School of Medicine, Boston, USA

Source PDF DOI Publisher page
183 days

Quantifying the Financial Return on Investment of Risk-Based Quality Management Implementation in Clinical Development

AuthorsAbigail Dirks; Sylviane de Viron; Kenneth McFarlane; Kenneth A. Getz

Affiliations1. Tufts Center for the Study of Drug Development, Tufts University School of Medicine, Boston, USA; 2. Clue Points S.A, Louvain-la-Neuve, Belgium; 3. CluePoints Inc, King of Prussia, USA

Source PDF DOI Publisher page
44 days

Identifying and Deploying Benchmarks for Clinical Research at Sites

AuthorsRida Momin; Laura Mangiarini; Alexandre Dias Tavares Costa; Carla Peacock; Emaad Shariff; Sara Noorain; Jennifer Preston; Sabah Attar

Affiliations1. Northern Care Alliance NHS Foundation Trust, Greater Manchester, UK; 2. Fondazione Penta ETS, Padova, Italy; 3. Instituto Carlos Chagas (ICC/Fiocruz Paraná), Rio de Janeiro, Brazil; 4. Innovate R Ltd., Manchester, UK; 5. Groundmark Learning, Leamington Spa, UK; 6. University of Liverpool, Liverpool, UK

Source PDF DOI Publisher page
104 days

Real-World Evidence for Drug Approvals: Moving Toward Greater Regulatory Clarity

AuthorsTala H. Fakhouri; Rasika Kalamegham; Nicole Mahoney; Rose Purcell; Mike D’Ambrosio

Affiliations1. Parexel International, Maryland, USA; 2. Genentech, Washington, DC, USA; 3. Novartis, Rockville, USA; 4. Takeda, Washington, DC, USA

Source PDF DOI Publisher page

Expert Matching · Case Demo

Turn Your Submission Goalsinto a Verifiable Journal Plan

Share your field, deadline, and author profile. CrushSCI uses real review records to suggest a title direction, shortlist journals, and estimate timelines.

CrushSCI online

Client

I work in environmental engineering and need an SCI paper published within three months. I have no grant funding or prominent co-author. Which journals could I target?

CrushSCI

Yes. We will first screen for feasibility against the 90-day deadline, then identify comparable papers without grant support or prominent co-authors. The final shortlist will prioritize research quality and journal scope.

Suggested title
Machine Learning and Life-Cycle Assessment for Predicting and Optimizing Carbon Emissions in Urban Wastewater Treatment

SampleLatest 5 valid paper samples from 2026

Average review96.4 days

Median77 days

Contact CrushSCI

Contact CrushSCI

Leave your contact details so we can discuss your manuscript, editing needs, and submission plan.

Selected service: Paper Editing Service

Or leave your contact details

WhatsApp, Telegram, WeChat, and email are all optional, but at least one is required. Once received, we will contact you as soon as possible.