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    Skolastika LLC

    Medical Research Consulting, Writing, Grants, Paper Publishing...

    Learn More
  • Slide 2

    Clinical Study Management, Study Monitoring

    Database Management, Software Programming

    Meet Our Team
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    Education, Public Health Policy, Sustainability

    Great Projects Take Great Writing

    About Us

SOME FEATURES

We offer scientific and medical editing services, which include dual editing process: the documents are first edited by experts in the specific discipline, followed by editing by our expert language reviewer. Our experts have advanced degrees (PhD, MS, or MBA) and years of experience in their areas of research. As we cover a wide range of disciplines, your editor will be selected to match the subject of your paper.


In addition to proofreading, we can format your documents to meet specific journal requirements, create figures and tables, embed images, and otherwise assist you to make your research results presentation effective and appealing.

MEDICAL WRITING

We offer a wide range of medical writing services including clinical study documents (see samples), abstracts, summaries, articles, book chapters, presentation kits, booklets, reports, training material, and guidelines.

GRANT EDITING

We have experience with grant proposal submissions to a number of federal agencies and can assist with formatting to meet the requirements of a specific agency. We can assist you in preparation of compelling proposals by improving organization and clarity, as well as with preparation of figures, tables, and graphs to effectively communicate your message.

PAPER WRITING

Our experts can save you time and improve the quality of your documents. We can assist you with manuscript organization, data presentation, clarity, and proofreading in order to obtain a polished, well-written manuscript ready for publication.

DATABASE

Our experts can save you time and improve the quality of your documents. We can assist you with manuscript organization, data presentation, clarity, and proofreading in order to obtain a polished, well-written manuscript ready for publication.

ABOUT US

Skolastika LLC support all aspects of your clinical research operations including preparation, initiation, conduct, monitoring, database building, management and close-out of clinical trials and other research projects. Our experience comming from work supporting pharmaceutical, medical device and educational institutions. Skolastika team has writing expertise and we are delivering well-constructed, high quality clinical documents including Protocols for clinical and research studies, Investigator brochures, Instruction for Use, Forms for clinical studies, Clinical Study final Reports (CSRs), Clinical Evaulation Reports (CERs), Literature Reviews, Post-Market plans and reports, Clinical Safety documents and many other types of required clinical documents. We are also experienced into Grant writing and publishing of study results and analyses in world leading scientific and medical magazines. Skolastika can help in developing plans and oversees critical regulatory activities in compliance with company policies, as well as local, United States and international regulations.

Skolastika offers flexibility, in-person assistance and ease of communication. It assures that your documents get the attention they deserve and that short deadlines can be met. We can also write documents in several languages, due to our US education and European origin. Skolastika also supports specific European Medical Device Regulatory requirements (EU MDR 2017/745 and 746) to ensure our client companies have compliant clinical support documentation.

We are SKOLASTIKA LLC

Medical Writing & Clinical Studies Support

Our experts are gathered from our family circle and have backgrounds in wide range of scientific, technical, and medical disciplines. Our professional experience includes years of writing projects and documents either for the institutions with which we were affiliated, or for those with whom we collaborated. The list of them is very impressive (ranging from the WHO and different universities, to NASA). We also worked with clients from the biotechnology and pharmaceutical industries. Please, check the PORTFOLIO section.

Behind Skolastika Inc is over 20 years of experience in writing peer-reviewed journal papers, review papers, book chapters, writing investigator brochures, presentations, grant proposals, and clinical study documents including synopses, protocols, informed consent documents, guidelines, SOPs, and reports (CERs, BERs, CSRs). We served as grant reviewers, journal article reviewers, IRB committee members, or have lead clinical studies.

Clinical Studies Documents (Protocol, Brochure, CSRs, CRFs) 100%
Regulatory Documents (CER, BER, IFUs, Audit preparation) 100%
Medical Publiching (Articles, Book Chapters) 80%
Research Study Grants 90%
Project Management 90%
Clinical Study Monitoring 90%
Database Managemant 90%

MEET THE TEAM

Skolastika was started by Miodrag Ognjanovic, MS in Public Health, who has over a decade of experience in oncology research, medical devices clincal studies and also participating in public health acitivities. Miodrag lead a number of international oncology studies innitiated by WHO agency for Cancer research (IARC) and also lead number of ICS related to medical devices working with 3M. He was often approached by his colleagues (both in and outside of the US) with requests for reviews and proofreading. They sought an expert who understood the science contained in their documents, and improve the clarity and impact of their documents.

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MIODRAG OGNJANOVIC


MS Public Health Policy
University of Minnesota Twin Cities
IOCPR Lead Investigator of IARC/WHO Research studies
Previous: 3M Health, University of Minnesota
Owner of Skolastika LLC

Skolastika build team for every project seeking expertise from members of our family and their close friends. We have backgrounds in wide range of scientific, technical, and medical disciplines. Our professional experience includes years of writing projects and documents either for the institutions with which we were affiliated, or for those with whom we collaborated. The list of them is very impressive (examples are: WHO, IARC, 3M, Medtronic, Edwards, Mayo Clinic, Microsoft, Baxter, Beckman Coulter, different universities and hospitals, NASA). We also worked with clients from the biotechnology and pharmaceutical industries. Please, check the PORTFOLIO and personal CVs section.

team 1

SIMONA


PhD Biomedicine
University of Hawaii
Director of Clinical Evidence, Balt USA
Previous: Medtronic Inc, Edwards Inc, University of Minnesota

team 3

MISHO


MBA, Bussines Management
Hawaii Pacific University
Lecturer, University of Hawaii
Previous: Economic attache, Serbian Embassy USA, Microsoft Inc

team 5

ALEKSA


BS Biomedical Enineering
University of Wisconsin Milwaukee
Senior Test Engineer, Baxter Inc
Previous: Systems Engineer Beckman Coulter

team 6

MARKO


MS Environmental Sustainability
University College Dublin Ireland
BS Sustainable Systems Management
University of Minnesota Twin Cities

PORTFOLIO

Our professional experience includes years of writing projects and documents either for the institutions with which we were affiliated, or for those with whom we collaborated. The list of them is very impressive (examples are: WHO, IARC, 3M, Medtronic, Edwards, Mayo Clinic, Microsoft, Baxter, Beckman Coulter, different universities and hospitals, NASA). We also worked with clients from the biotechnology and pharmaceutical industries.

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We have experience with grant proposal submissions to a number of federal agencies and can assist with formatting to meet the requirements of a specific agency. We can assist you in preparation of compelling proposals by improving organization and clarity, as well as with preparation of figures, tables, and graphs to effectively communicate your message. We offer a wide range of medical writing services including clinical study documents (see samples), abstracts, summaries, articles, book chapters, presentation kits, booklets, reports, training material, and guidelines.

team 1
Clinical Studies

• Childhood Cancer Protocol (Sample)
• Neonatel Questionnaire...(Sample)
• Biospecimens Protocol...(Sample)
• List of (Clinical)
team 3
Grant Samples

• Grant Sample: Rhabdomyosarcoma (RMS) (Document)
• ​Grant Sample: Li-Fraumeni Syndrom (Document)
• Grant Sample: Astrobiology (Document)
• List of (Grants)
team 5
Publications

• Comprehensive Toxicology (Book Chapter)
• Genomic organization of the gene coding...(Paper 2001)
• Clinical utility of circulating tumor...(Paper 2012)
• Analgesic use during pregnancy...(Paper 2011)
• List of (Publications)
team 6
Regulatory

• Nanotechnology Safety Guide (Sample)
• Pyrophoryc Flyer...(Sample)
• Clinical utility of circulating tumor...(Paper 2012)
• List of (Regulatory)
team 6
Engineering

• Comprehensive Toxicology (Book Chapter)
• Genomic organization of the gene coding...(Paper 2001)
• Clinical utility of circulating tumor...(Paper 2012)
• List of (Engineering)
team 6
Sustainability

• Comprehensive Toxicology (Book Chapter)
• Genomic organization of the gene coding...(Paper 2001)
• Clinical utility of circulating tumor...(Paper 2012)
• List of (Sustainability)

CONTACT US

We would like to talk with you. Find us on social networks pages, send us email or give us a call. If you are around, stop and visit us. We are here to hear your ideas and to understand your needs.

OUR ADDRESS

+1 612 245-7455

info@skolastika.com

www.skolastika.com

540 Woodhill Dr, Roseville, MN 55113