Our Services

Clinical Trial Management

Clinical Trial Management can involve thousands of people, hundreds of investigative sites, multiple CROs and various clinical source systems - all generating huge amounts of data. Our Clinical research associates overseas the each study of the clinical process to ensure proper planning, conduct, patient safety, data quality. Clinical trial Management is a site management which requires the maximum no. Of subjects. Our CTM is a powerful end-to-end clinical trial management solution that provides control, efficiency and quality data to every study For this process they require Clinical Research Associate (CRA) which takes a major part.CRA major work is to gather, collect and maintain all the subjects information manually.

  • Study document development
  • CRA Management and quality control
  • Clinical Monitoring and site management
Clinical Data Management

The process of managing documents and other types of information such as images from creation, review, storage to its dissemination. It also involves the indexing, storage and retrieval of documents in an organized method.

  • Improve the speed of your business by accessing and using information.
  • improve operational effectiveness with simplified processes.
  • Optimize your company's performance.
  • Management of incoming and outgoing documents, structured and unstructured data sources.
  • Reliable and secure archives.
  • Scalable and robust easy to locate the right document.

The role of Bio-Statistics is the key to the successful planning and execution of a development program. Bio-Statistics are referred as extracting and clean the data. We can provide adequate advice for the calculation of sample size, randomization programs, statistical analysis plans (SAP), data interpretation and more. We are using bio statistics for Creation of Statistical Analysis Report. We are using different programming languages to extract the data which are mainly include Saas 4.4 base version and R programming language. For the analysis of data with softwares, we are using different tests like Z- Test, T-Test, chi square test.

Medical Writing

Medical writing is an integral part of clinical research. Our medical writers work closely with our colleagues in the bio statistic, pharmacovigilance, project management and clinical data management teams to provide accurate, timely and inexpensive documents to the highest ethical and scientific standards. Sclin Soft Technologies offers a complete range of medical writing services for regulatory mailings, scientific communications and medical-marketing materials in different therapeutic areas for all phases of the product life cycles, from preclinical development to post-marketing literature.We guarantee the timely delivery of precise, regular and regulatory-compliant documents to our sponsors in an affordable and flexible way. We organize our operations in integrated customer-centric units, to improve customer focus and to guide operational agility that can lead to delivery with quality, speed and value.The medical writers of the Sclin Soft Technologies team receive regular training to ensure uniform uniformity with regulatory standards and to have consistency between writing processes. Our medical authors are scientists involved in the development of drugs that have the required scientific background, regulatory knowledge and professional attitude to be incorporated into the sponsor's study teams during the clinical development process of a molecule.

  • Journal articles - Original research, Review articles, Editorials, case reports, etc.
  • Attract and retain quality, high-paying customers
  • Abstracts- Publication in journals and Submission to medical meetings
  • Posters Presentation at medical meetings
Patent Services

The purpose of patent services is to spread the knowledge and importance of opportunities in identification, intellectual property and regulatory affairs and to cultivate the culture of these assets in an organization to create brand value for the organization. We are experts in patent filing, i.e. intellectual property in the areas of chemical, pharmaceutical, ethical and generic products, software and hardware, etc. These intellectual properties are intangible assets that maximize the generation of revenue through the correct and effective exploitation of the knowledge acquired.

Patent Services
  • Regulatory consultant for medicines, pharmaceutical products, veterinary medicines, medical devices and food supplements
  • Submission of the patent (Indian and global)
  • PCT is archiving
  • Preparation of ANDA certifications for USA, CA, AU.
  • brands..
  • Copyright
  • Drawings

Sclintech has a experience with scanning and sorting of clinical records, HR Records, Bank documents, land records, legal documents in fact any physical records get digitized with 100% accuracy and perfection. We transform all paper copies into digital format irrespective of the size of the paper.

Our EMR (Electronic Medical Records) scanning solutions

- Sclintech is expert in EMR (Electronic Medical Records) processes that convert everything into digital format so that hospital staff, doctors, and medical offices can access them easily. No hassles of managing piles of papers manually. Our solution makes operations easy and efficient so that you save time and resources.

- Our team arranges physical papers in a systematic form before forwarding to the digitization process. They fix the imperfections, correct the rips or ragged edges and align them in the best possible manner. The records are scanned and converted into digital images. Our reliable servers save the digitized images in high-end secure servers.

- Assign the task of digitizing to Sclintech and relax in a better way. Our scanning and storing systems are safe, fast and extremely reliable.