(Pioneering Your Path to Clinical Excellence)

                                                Your Transparent, Committed & Reliable Partner in Life Science Industries.

At Tuliphall CliniResearch Private Limited, we’re all about making clinical trials smoother and more effective. Think of us as your go-to partner, guiding you from the very first brainstorming session all the way to the finish line when you get that all-important approval. Our team is committed to upholding high standards throughout every step of the process, ensuring that your clinical trials are not just successful, but also efficient and reliable.

Vision:

At Tuliphall CliniResearch, envision with a focus on collaboration and transparency, we strive to be the trusted partner in the clinical research landscape, paving the way for safer and more effective healthcare system for all.

Mission:

Our mission at Tuliphall CliniResearch is to turn medical advancements from dreams into reality. We offer a full suite of services, from strategic planning and regulatory submissions to the nitty-gritty of clinical operations. Our team’s expertise and unwavering commitment to excellence ensure that every clinical trial is more than just a checkbox—it’s a meaningful journey towards approval and enhanced patient care. We believe in the power of teamwork, open communication, and a personal touch because, at the end of the day, every trial represents real people and their stories. Let’s make a difference together!

We provide services from initial strategic planning through regulatory submissions, full clinical operation until approval. We are dedicated to ensuring that each clinical trial is executed to the highest possible standards. Our core competencies are in following areas:-

               Product  Registration support 

               Trial Design,

               Site Selection,

               Project/Site Management,

               Med-tech Solutions,

               Patent Filing

                Data Management,

                Biostatistical Analysis,

                Medical Writing,

                Clinical Quality Development,

                Pharma Analytics,

                RWE Solutions,

                Consultation Services,

CLINICAL OPERATION

Our clinical operations team is highly experienced and trained in effective site management services, ranging from feasibility study to study close-out. Collectively, the team has vast experiences in several therapeutic areas. We ensure the best clinical services, highest ethical standard and quality clinical data.

PROJECT MANAGEMENT

We consider our success in the success of our Clients project. We work as a strategic partner to complement your team. We are experienced in the management of clinical studies in all phases I-IV, in all major therapeutic indications.

SITE MANAGEMENT

A thorough feasibility and site selection is the basis of any successful clinical trial. Our feasibility group has worked on virtually every therapeutic area. Our study feasibility assessment process is efficient and is capable of identifying the best investigative sites to conduct a clinical trial.

 PROTOCOL DEVELOPMENT

A well-designed set of Standard Operating Procedures (SOPs) can improve efficiency, lower costs, elevate compliance, clarify team roles, reduce training requirements, raise quality, improve safety, and enhance your ability to troubleshoot and correct problems.

SITE MONITORING

We provide comprehensive site monitoring and management. Our Clinical Research Associates (CRAs) act as the liaison between the sites and the study team. Our CRAs are assigned to specific sites for the duration of the study to provide consistent support for sites. All monitoring activities are conducted in accordance with GCP/ICH Guidelines and follow CDSCO/FDA/EMEA regulations.

REGULATORY AFFAIRS

We support our client’s product development programs by playing a pivotal role in obtaining regulatory approvals in the shortest possible time. We have a dedicated in-house regulatory team which assists in a broad range of Regulatory Consultations for most effective approvals and strategies.

DATA MANAGEMENT

Our primary goal in data management is to provide clean, locked databases, in a suitable format, on time and on budget. Clinical Data Management (CDM) team experts are committed to upholding a standardized, process-driven approach.

PHARMACOVIGILANCE

TCR offers pharmacovigilance solutions for clinical safety, post-market surveillance and risk management or risk minimization plans. Our Medical Affairs team is composed of experienced clinical professionals who analyze the safety profile of their products throughout all the phases of clinical development and post-marketing.

MEDICAL WRITING & TRANSLATIONS

Medical Writers have medical, pharmaceutical and life science backgrounds and are experienced in producing high quality Phase I–IV clinical documentation across a wide range of therapeutic areas that strictly adhere to ICH-GCP guidelines and local regulatory requirements. We understand the importance of communicating the details clearly, concisely, and accurately.

QUALITY ASSURANCE

Quality Assurance includes all planned and systematic evaluations necessary to ensure that all quality requirements are fulfilled and that a trial is conducted, the data generated, documented (recorded) and reported in compliance with GCP and regulatory requirements.

BIOANALYTICAL

All assays and methods are validated according to US-FDA guidelines. In addition to providing support for in-house clinical pharmacology activities, our bioanalytical unit also routinely provides support for clinical studies conducted at other sites.

OBSERVATIONAL/ NON INTERVENTIONAL STUDIES

Observational studies are performed for approved drugs within the standard therapy. Usually, these studies are intended for the documentation of the use of a drug under “field conditions”, i.e. without the “experimental bias” of clinical studies.

Clinical Research Training Courses

We are dedicated and committed to provide ‘The Best Professionals’ to the Clinical Research Industry. To meet the increasing demands of professionals in the field of Clinical Research, we built up a talent pool, consisting of ‘Experienced Professional Faculties’; who are committed to fulfill the challenge to meet the industry demands.