Themedical writing services team at Cognibrain comes distinctively qualified to research, compile, write and edit a wide range of medical specialties and scientific areas that are required to support your content development efforts.
Medical writing is the art of creating a document that includes medical information in a readable language which is easily comprehended by the target audience. The target audience for medical writing varies and so is the style of medical writing.
https://www.cognibrain.com/medical-writing-answering-your-questions/
Medical writing involves producing scientific documentation for clinical research in a clear, standardized manner. It includes regulatory writing for submissions to authorities, educational writing for various audiences, and medical marketing. Good medical writers have scientific backgrounds and abilities to research topics, think logically, and communicate complex information clearly to different audiences. They follow steps like reviewing information and receiving approvals when writing documents and ensure compliance with relevant guidelines and regulations.
This document discusses the clinical trials process from protocol development through study completion. It covers developing the protocol, regulatory documents, patient recruitment, safety reporting, interim reports, and end of study activities. Key aspects include writing an approvable protocol, establishing an investigator site file, screening and enrolling suitable patients, maintaining safety oversight, and conducting closeout procedures. The goal is to provide guidance on managing all stages of a clinical trial.
This document provides an overview of medical writing, including:
- Defining medical writing as applying clinical research principles to develop documents that clearly describe research results and medical information.
- Outlining the different types of medical writing such as regulatory, educational, and publication/presentation.
- Explaining that medical writing emerged in the pharmaceutical industry to produce well-structured documents that present complex clinical trial information clearly.
- Detailing the skills required for medical writing like domain knowledge, statistics, writing ability, and understanding guidelines.
The document discusses case report forms (CRFs), which are used in clinical trials to record patient data. It defines CRFs and explains that they contain all protocol-required information including adverse events. The goals of CRFs are to collect verifiable data according to Good Clinical Practice standards. CRFs can be paper-based or electronic. Well-designed CRFs are structured and formatted consistently to facilitate accurate data collection while avoiding duplication. CRFs provide essential standardized data that is analyzed to advance medical research.
Medical writing is the art of creating a document that includes medical information in a readable language which is easily comprehended by the target audience. The target audience for medical writing varies and so is the style of medical writing.
https://www.cognibrain.com/medical-writing-answering-your-questions/
Medical writing involves producing scientific documentation for clinical research in a clear, standardized manner. It includes regulatory writing for submissions to authorities, educational writing for various audiences, and medical marketing. Good medical writers have scientific backgrounds and abilities to research topics, think logically, and communicate complex information clearly to different audiences. They follow steps like reviewing information and receiving approvals when writing documents and ensure compliance with relevant guidelines and regulations.
This document discusses the clinical trials process from protocol development through study completion. It covers developing the protocol, regulatory documents, patient recruitment, safety reporting, interim reports, and end of study activities. Key aspects include writing an approvable protocol, establishing an investigator site file, screening and enrolling suitable patients, maintaining safety oversight, and conducting closeout procedures. The goal is to provide guidance on managing all stages of a clinical trial.
This document provides an overview of medical writing, including:
- Defining medical writing as applying clinical research principles to develop documents that clearly describe research results and medical information.
- Outlining the different types of medical writing such as regulatory, educational, and publication/presentation.
- Explaining that medical writing emerged in the pharmaceutical industry to produce well-structured documents that present complex clinical trial information clearly.
- Detailing the skills required for medical writing like domain knowledge, statistics, writing ability, and understanding guidelines.
The document discusses case report forms (CRFs), which are used in clinical trials to record patient data. It defines CRFs and explains that they contain all protocol-required information including adverse events. The goals of CRFs are to collect verifiable data according to Good Clinical Practice standards. CRFs can be paper-based or electronic. Well-designed CRFs are structured and formatted consistently to facilitate accurate data collection while avoiding duplication. CRFs provide essential standardized data that is analyzed to advance medical research.
AN OVERVIEW AND IMPORTANCE OF PHARMACOVIGILANCERamakrishna K
An introduction to pharmacovigilance, basic types like active pharmacovigilance and passive pharmacovigilance, purpose, adverse event reporting, data processing, causality, assessement, signal detection, risk management plans and analysis
Table of contents
-Definition of CRF
-What is CRF
-Types & Methods of filling of CRF
-CRF Input team
-CRF Approval team
-Review team
-Facts about CRF
-Purpose of CRF
-CRF Development process & Guidelines
-Elements of CRF
-CRF Design
-CRF completion checklist
-CRF Design tools
-CRF use
-GCP connection
Patient recruitment & retention is highlighted as the key factor in ensuring study success, the area of patient retention in clinical trials is often overlooked. Retention of patients throughout the life of a clinical trial is however extremely vital from scientific as well as economic point of view. Poor recruitment & retention negatively impacts on the overall evaluable data for regulatory submissions. Dropped participants must be replaced which incurs further expenditures and time delays. Subject dropout rates are estimated to range from 15-40% of enrolled participants in clinical trials.
MedDRA - the Medical Dictionary for Regulatory Activities - is a medical terminology used to classify adverse event information associated with the use of biopharmaceuticals and other medical products (e.g., medical devices and vaccines). Coding these data to a standard set of MedDRA terms allows health authorities and the biopharmaceutical industry to more readily exchange and analyze data related to the safe use of medical products.
This document defines and describes the role and responsibilities of an Institutional Review Board (IRB). The key points are:
1) An IRB is responsible for reviewing and approving research involving human subjects to ensure ethical standards are met and subjects' rights and safety are protected.
2) IRBs must have diverse and qualified membership, including scientific and non-scientific experts, to conduct in-depth reviews of research protocols.
3) The IRB review process involves evaluating research protocols, consent forms, recruitment procedures and investigators to ensure all applicable regulations and ethical guidelines are followed.
In this presentation, Brandon May, freelance medical writer and owner of May Medical Communications, LLC, describes 5 types of medical writing.
Read the blog post that accompanies this slide deck at http://maymedcomm.com/5-different-types-of-medical-writing/
PMS are the studies done after the drug is marketed to ensure the safety and efficacy of drugs. Here detailed about the need for PMS, sources of informations and methods of PMS
Regulatory medical writing is an integral part of Medical Communications, but is often overlooked. In simple terms, it involves writing of the documents required for the approval of drugs by the regulatory authorities.
https://www.cognibrain.com/regulatory-medical-writing/
The document provides guidance on preparing Developmental Safety Update Reports (DSURs). It outlines the objectives, scope, periodicity and format of DSURs. Key information to include in a DSUR are estimated clinical trial exposure, safety data from trials, actions taken for safety reasons, changes to the reference safety information, and an overall safety assessment. The DSUR is intended to provide regulators with the latest safety information on investigational products.
The document discusses medical writing, which involves producing scientific documentation for researchers who are not directly involved in the studies. It describes the need for medical writing due to the complex nature of clinical trials and regulations. There are two main types of medical writing - regulatory, which creates documents for approval processes, and educational, which makes information accessible to healthcare professionals and the public. Medical writers require skills like attention to detail, writing ability, and scientific knowledge. Their duties can include drafting protocols, reports, and manuscripts for publication.
The clinical research associate (CRA), also known as the monitor, acts as the main line of communication between the sponsor and investigator. The CRA is responsible for evaluating investigators to ensure they are qualified through training and experience and have adequate resources to properly conduct the trial. Additional responsibilities include conducting pre-study visits to assess investigator experience and facilities, site initiation visits to detail study obligations, and routine monitoring visits to ensure subjects' rights and data accuracy and compliance with regulations. The CRA also performs site closeout visits when enrollment and subjects' activities are complete and data are finalized.
Roles and Responsibilities of sponsor in conducting clinical trials as per GC...Dr B Naga Raju
Presentation on Roles and Responsibilities of sponsor in conducting clinical trials as per GCP-ICH for pursuing a subject in the course of PharmD programme under RGUHS
This document provides an introduction to post-marketing drug safety surveillance conducted by the FDA's Center for Drug Evaluation and Research (CDER). It defines pharmacovigilance and describes the Division of Pharmacovigilance's key roles in postmarketing safety monitoring, including collecting and analyzing adverse event reports from healthcare providers and patients. Spontaneous reporting systems like FDA Adverse Event Reporting System (FAERS) are useful for detecting rare or long-term safety issues not seen in clinical trials. The division evaluates safety signals and can recommend actions such as label changes or risk management plans based on its analyses.
Essential Documents of Clinical Trials_2heba rashed
Essential documents for clinical trials include documents that demonstrate compliance with good clinical practice standards and regulations. These documents are grouped into three sections: before, during, and after the clinical trial. Key documents include the protocol, patient consent forms, safety reports, data records, and archival documents that must be retained for 15 years. Maintaining organized essential document files is important for evaluating trial conduct and data quality.
The CRA oversees all stages of clinical trials from site selection to completion. They identify investigators, set up trial sites, train staff, monitor compliance, and verify informed consent and data collection. The CRA ensures protocols are followed, documents are collected, and supplies are accounted for throughout the trial. Effective communication, relationship building, attention to detail, and strong organizational skills are important for this role.
An brief introduction to the clinical data management process is described in this slides. These slides provides you the information regarding the data evaluation in the clinical trials , edit checks and data review finally data locking,then the data is submitted to the concerned regulatory body.
Clinical trial protocol, ammendments, Protocol deviations and violationsAmol Patil
This document provides guidelines for developing a clinical trial protocol including general information, background, aims and objectives, inclusion/exclusion criteria, study design, methodology, statistics, ethics, quality control, and protocol amendments. Key elements that must be addressed in the protocol are enumerated such as the research question, treatment characteristics, data collection and analysis, and legal responsibilities. Protocol deviations and violations that occur during the study are also discussed along with examples and regulatory requirements for reporting them. Adherence to good clinical practice and obtaining necessary approvals are emphasized.
Medical and Scientific Writing Services in South Africa.pptxnancymartinez402574
If you are a researcher, physician, or other professional in the medical or scientific sector, you understand the importance of creating clear, concise, and accurate communications. With so much on your plate, however, it might be tough to find the time to produce all of the necessary documentation, such as research papers, grant proposals, clinical trial reports, and regulatory submissions.
Medical and Scientific Writing Services in the UK.pptxJohn William
Medical and scientific writers In Oxford have the knowledge, experience, and abilities to write about complicated subjects in a clear, concise, and accurate manner. They may also assist you in tailoring your writing to the specific needs of your target audience and ensuring that your work complies with all applicable regulations.
AN OVERVIEW AND IMPORTANCE OF PHARMACOVIGILANCERamakrishna K
An introduction to pharmacovigilance, basic types like active pharmacovigilance and passive pharmacovigilance, purpose, adverse event reporting, data processing, causality, assessement, signal detection, risk management plans and analysis
Table of contents
-Definition of CRF
-What is CRF
-Types & Methods of filling of CRF
-CRF Input team
-CRF Approval team
-Review team
-Facts about CRF
-Purpose of CRF
-CRF Development process & Guidelines
-Elements of CRF
-CRF Design
-CRF completion checklist
-CRF Design tools
-CRF use
-GCP connection
Patient recruitment & retention is highlighted as the key factor in ensuring study success, the area of patient retention in clinical trials is often overlooked. Retention of patients throughout the life of a clinical trial is however extremely vital from scientific as well as economic point of view. Poor recruitment & retention negatively impacts on the overall evaluable data for regulatory submissions. Dropped participants must be replaced which incurs further expenditures and time delays. Subject dropout rates are estimated to range from 15-40% of enrolled participants in clinical trials.
MedDRA - the Medical Dictionary for Regulatory Activities - is a medical terminology used to classify adverse event information associated with the use of biopharmaceuticals and other medical products (e.g., medical devices and vaccines). Coding these data to a standard set of MedDRA terms allows health authorities and the biopharmaceutical industry to more readily exchange and analyze data related to the safe use of medical products.
This document defines and describes the role and responsibilities of an Institutional Review Board (IRB). The key points are:
1) An IRB is responsible for reviewing and approving research involving human subjects to ensure ethical standards are met and subjects' rights and safety are protected.
2) IRBs must have diverse and qualified membership, including scientific and non-scientific experts, to conduct in-depth reviews of research protocols.
3) The IRB review process involves evaluating research protocols, consent forms, recruitment procedures and investigators to ensure all applicable regulations and ethical guidelines are followed.
In this presentation, Brandon May, freelance medical writer and owner of May Medical Communications, LLC, describes 5 types of medical writing.
Read the blog post that accompanies this slide deck at http://maymedcomm.com/5-different-types-of-medical-writing/
PMS are the studies done after the drug is marketed to ensure the safety and efficacy of drugs. Here detailed about the need for PMS, sources of informations and methods of PMS
Regulatory medical writing is an integral part of Medical Communications, but is often overlooked. In simple terms, it involves writing of the documents required for the approval of drugs by the regulatory authorities.
https://www.cognibrain.com/regulatory-medical-writing/
The document provides guidance on preparing Developmental Safety Update Reports (DSURs). It outlines the objectives, scope, periodicity and format of DSURs. Key information to include in a DSUR are estimated clinical trial exposure, safety data from trials, actions taken for safety reasons, changes to the reference safety information, and an overall safety assessment. The DSUR is intended to provide regulators with the latest safety information on investigational products.
The document discusses medical writing, which involves producing scientific documentation for researchers who are not directly involved in the studies. It describes the need for medical writing due to the complex nature of clinical trials and regulations. There are two main types of medical writing - regulatory, which creates documents for approval processes, and educational, which makes information accessible to healthcare professionals and the public. Medical writers require skills like attention to detail, writing ability, and scientific knowledge. Their duties can include drafting protocols, reports, and manuscripts for publication.
The clinical research associate (CRA), also known as the monitor, acts as the main line of communication between the sponsor and investigator. The CRA is responsible for evaluating investigators to ensure they are qualified through training and experience and have adequate resources to properly conduct the trial. Additional responsibilities include conducting pre-study visits to assess investigator experience and facilities, site initiation visits to detail study obligations, and routine monitoring visits to ensure subjects' rights and data accuracy and compliance with regulations. The CRA also performs site closeout visits when enrollment and subjects' activities are complete and data are finalized.
Roles and Responsibilities of sponsor in conducting clinical trials as per GC...Dr B Naga Raju
Presentation on Roles and Responsibilities of sponsor in conducting clinical trials as per GCP-ICH for pursuing a subject in the course of PharmD programme under RGUHS
This document provides an introduction to post-marketing drug safety surveillance conducted by the FDA's Center for Drug Evaluation and Research (CDER). It defines pharmacovigilance and describes the Division of Pharmacovigilance's key roles in postmarketing safety monitoring, including collecting and analyzing adverse event reports from healthcare providers and patients. Spontaneous reporting systems like FDA Adverse Event Reporting System (FAERS) are useful for detecting rare or long-term safety issues not seen in clinical trials. The division evaluates safety signals and can recommend actions such as label changes or risk management plans based on its analyses.
Essential Documents of Clinical Trials_2heba rashed
Essential documents for clinical trials include documents that demonstrate compliance with good clinical practice standards and regulations. These documents are grouped into three sections: before, during, and after the clinical trial. Key documents include the protocol, patient consent forms, safety reports, data records, and archival documents that must be retained for 15 years. Maintaining organized essential document files is important for evaluating trial conduct and data quality.
The CRA oversees all stages of clinical trials from site selection to completion. They identify investigators, set up trial sites, train staff, monitor compliance, and verify informed consent and data collection. The CRA ensures protocols are followed, documents are collected, and supplies are accounted for throughout the trial. Effective communication, relationship building, attention to detail, and strong organizational skills are important for this role.
An brief introduction to the clinical data management process is described in this slides. These slides provides you the information regarding the data evaluation in the clinical trials , edit checks and data review finally data locking,then the data is submitted to the concerned regulatory body.
Clinical trial protocol, ammendments, Protocol deviations and violationsAmol Patil
This document provides guidelines for developing a clinical trial protocol including general information, background, aims and objectives, inclusion/exclusion criteria, study design, methodology, statistics, ethics, quality control, and protocol amendments. Key elements that must be addressed in the protocol are enumerated such as the research question, treatment characteristics, data collection and analysis, and legal responsibilities. Protocol deviations and violations that occur during the study are also discussed along with examples and regulatory requirements for reporting them. Adherence to good clinical practice and obtaining necessary approvals are emphasized.
Medical and Scientific Writing Services in South Africa.pptxnancymartinez402574
If you are a researcher, physician, or other professional in the medical or scientific sector, you understand the importance of creating clear, concise, and accurate communications. With so much on your plate, however, it might be tough to find the time to produce all of the necessary documentation, such as research papers, grant proposals, clinical trial reports, and regulatory submissions.
Medical and Scientific Writing Services in the UK.pptxJohn William
Medical and scientific writers In Oxford have the knowledge, experience, and abilities to write about complicated subjects in a clear, concise, and accurate manner. They may also assist you in tailoring your writing to the specific needs of your target audience and ensuring that your work complies with all applicable regulations.
This document provides information about medical dissertation writing services. It discusses the expertise of their writers in various medical fields over the past decade. Services include full medical thesis writing assistance from topic selection to conclusion, as well as editing, research paper publication support, and manuscript writing for journal submission. Key parts of a medical thesis and the editorial review process are outlined. Contact information is provided at the end.
Ryan Lilly of Matter and Tara Auclair of Modernizing Medicine's HITMC presentation: “How to Build a Diverse Media-Facing Thought Leadership Bench” took place on Thursday, April 5 at the New Orleans Marriot. Attendees learned how specialty-specific health IT leader, Modernizing Medicine, partnered with Matter to create engaging and impactful platforms for its spokespeople.
This document discusses medical writing, including its definition, types, need, required skills, duties of medical writers, and medical writing organizations. Medical writing involves producing scientific documentation for research performed by doctors and scientists. It emerged in the pharmaceutical industry due to the specialized skills needed to clearly present complex clinical trial information. The two main types are regulatory medical writing for approval documents, and educational writing for general audiences. Medical writing is needed due to the complexity of research and trials. Key skills include attention to detail, strong writing abilities, and scientific knowledge. Medical writers prepare documents for regulatory submissions and publications, and work to ensure clear communication of information. Several organizations support medical writers internationally.
This document describes the services of a firm that provides writing support for medical dissertations. They aim to deliver original medical content to PhD students and support clients with developing high-quality theses, manuscripts, and research papers. Their services include assistance with topic selection, formatting, editing, referencing, publishing, and covering a wide range of medical subjects including public health, nutrition, nursing, biotechnology, and more. They employ medical experts to offer specialized guidance to clients.
The document discusses the role of an internal consultant and the key aspects required to be successful in that role. It covers the necessary mindset, knowledge, process skills, and competencies. Specifically, it emphasizes the importance of strategic thinking, understanding complex problems, developing strong relationships and trust with clients, and having expertise in various shared competencies like communication, decision-making, and maintaining a positive outlook. The document provides examples of how to establish initial contact with clients, understand their needs, and manage the consulting process and relationship to deliver high quality service.
Fundamentals of Effective Business CommunicationWaleed Liaqat
The presentation describes how to communicate effectively in the business world today. Content has been extracted from "Business Communication Today" (9 ed.)
Medical writing involves clearly communicating clinical and scientific data in written form for various audiences. A medical writer uses their understanding of science and medical subjects combined with strong writing skills to present information at an appropriate level for the target reader. There are many types of medical writing including scientific, regulatory, medico-marketing, consumer, social media, and e-learning. To be a successful medical writer requires qualities like attention to detail, strong research abilities, effective communication skills, and a willingness to continuously learn. Following a four step writing process of prewriting, drafting, revising, and refining can help medical writers produce error-free documents that meet readers' needs.
The document discusses the roles and responsibilities of PhD supervisors, collaborators, and how to apply for NIHR funding. It provides the following key points:
1) PhD supervisors guide students through the process, ensure regulations are followed, help with contacts and research guidance, but do not do work for students or take responsibility for their research.
2) Students should carefully select 1-2 supervisors and a clinical supervisor, considering their accessibility, support, time availability, and experience.
3) Collaborators assist with specialist parts of a project and expect to be authors on related papers.
4) NIHR applications require selling yourself as a future research leader and securing university support well in advance of
The art and craft of writing successful proposalsAmjad Idries
The document provides guidance on writing successful grant proposals. It discusses important elements like clearly outlining the proposal idea, needs statement, objectives, budget, and following guidelines. Key recommendations include starting with a good idea aligned with funder priorities, improving packaging through logical organization and clear writing, and obtaining feedback from others. Common mistakes involve poorly addressing reviewer criteria, inconsistent sections, and weak justification. The document emphasizes conveying a proposal's significance and developing specific, measurable goals to convince reviewers of its merits.
Presented at the 2014 Los Angeles County Psychological Association's Convention. Basics of ethical paperwork in private practice for mental health professionals.
This document discusses leadership and provides advice for becoming an effective leader. It begins by defining leadership as influencing others to accomplish common goals. It then discusses the importance of having a clear mission and vision. The rest of the document offers tips on different leadership styles, developing emotional intelligence, acquiring leadership skills, dealing with stress, and caring for yourself as a leader. Overall, the key message is that strong leadership requires having a vision, adapting your style to situations, developing self-awareness, and supporting others.
Positive thinking, motivation, and learning skills are important life and professional skills. Positive thinking involves expecting good outcomes and believing in one's abilities. It benefits both mental health and relationships. Self-motivation helps accomplish tasks without relying on others through setting goals, seeking feedback, and dealing with obstacles. Research, another important skill, involves finding, analyzing, and evaluating information to solve problems or develop new ideas and products.
All About Translating ANOCs, EOCs, SBCs WebinarVIA, Inc.
During this webinar, we talked about:
*Scheduling your work in order to meet tight deadlines
*How to use our online translation portal to streamline your approval process
*How to reduce costs by using a translation memory (TM)
Along with other tips and best practices we’ve gathered from our years of open-enrollment translation work.
How to Write an Issue Paper and Analysis: A Stepwise Guide. 8 issue Paper Template - SampleTemplatess - SampleTemplatess. Writing an issue paper. How Do You Write an Issue Paper?. 2019-03-03. How to write a legal issue paper format: Term Paper. How to write an issue analysis paper. How to Write a Controversial .... social issue topics for research papers 28 images research paper topics .... Policy Issue Paper Example : Writing a Paper: Outlining. Policy Issue Paper Example - Organizing Your Social Sciences Research Paper. Issue analysis Research Paper Example Topics and Well Written Essays .... Issue paper outline. Outline of Issues Paper. 2019-02-02. 002 Gre Issue Essay Samples Maxresdefault Thatsnotus. Writing About Enduring Issues: Essay Which Matters Pro Essay Help. Issue Brief Template. Issue Paper 1-4.pdf DocDroid. How to Write an Issue Paper. Writing an issue paper. How to write an issue paper by Waterman .... How to write an issue paper. How to Write a Proposal Essay/Paper .... Magnificent Buy Essay Papers Thatsnotus. How to Write a Research Paper for Publication: Outline, F
A cv for life science december 9 2014 focused seminarMentLife
This document provides advice on creating an effective curriculum vitae (CV) for applications in both industry and academia. It emphasizes that CVs for industry should be concise and highlight transferable skills over specialized knowledge. Companies seek candidates with strong communication and problem-solving abilities who have researched the company and role. The cover letter is also important for customizing applications to specific jobs. CVs should make a good first impression and tell a story about the applicant's qualifications and fit for the opportunity.
,
preparing informative and influential report
,
report writing
,
determining the report purpose
,
determining the factors
,
general guideline for conducting a research
,
appropriate attitudes and practices
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researching and writing report
Do you think journal publication is an easy process?
You write a research paper, submit it to the journal office and Voila! The editors will publish your paper.
If you think so, you are mistaken. Submitting your paper for publication in your desired journal can be tedious as many things need to be taken care of.
https://www.cognibrain.com/dos-and-donts-when-submitting-your-research-paper/
Medical writers are an important link between medical technology and people. Medical writers may either be ‘in-house’ or ‘freelance’.
https://www.cognibrain.com/medical-writing-answering-your-questions/
ARRIVE guidelines provides a list of information that should be incorporated in reporting research in a scientific article related to animals. 20 items should be reported in the articles. To increase its validity and authenticity, the ARRIVE guidelines are prepared by taking inputs from researchers, journal editors, research funders, and statisticians.
https://www.cognibrain.com/arrive-guidelines-for-preclinical-studies/
Academic search engines are preferred over general search engines for research as they only search predefined academic journals, reviews and abstracts, ensuring higher quality results. General search engines search entire databases including irrelevant articles, have less organized results that lack standards. Academic search engines also provide advanced search options, allow determining research quality, and have specialized subdivided databases not available in general search engines.
Google scholar search provides more relevant academic search results as compared to normal google search. Unlike normal Google search, the Google scholar search avoids the general articles or articles from unreliable sources in the search result.
https://www.cognibrain.com/using-google-scholar-in-the-best-way/
Through academic search engines, the researchers can gain access to reliable and authentic information with ease. Reasons for searching through academic search engines are:
https://www.cognibrain.com/top-academic-search-engines-for-research/
Google Scholar is an academic search engine. It is a subset of the normal google search. It provides academic results including research articles from reliable sources.
https://www.cognibrain.com/using-google-scholar-in-the-best-way/
There are several types of academic search engines that can help researchers find scholarly articles and publications. CORE indexes hundreds of thousands of research articles from institutions and open access journals. Google Scholar provides millions of articles, books, theses, and dissertations from its large database. Microsoft Academic searches millions of publications and presents search results with graphs and charts. The BASE search engine contains over 150 million documents from over 7000 sources, with 60% available in full text. Semantic Scholar uses artificial intelligence to provide optimized search results and was launched in 2015. CiteSeerX aims to improve dissemination of scientific information and provides freely accessible articles. Science.gov contains over 200 million pages across 60 databases and 2200 websites
The Good Publication Practice Guidelines provide recommendations about the publications of research studies that are sponsored by the pharmaceutical, biotechnological, and diagnostic companies.
https://www.cognibrain.com/communicating-company-sponsored-medical-research-following-good-publications-practice/
The document discusses guidelines for good publication practice in company-sponsored medical research. It outlines recommendations for publishing research studies sponsored by pharmaceutical and biotech companies. Key aspects of the guidelines include completeness in reporting all data findings, following relevant regulatory laws and ethical guidelines, ensuring collaboration between authors, and disclosing conflicts of interest. Adhering to these guidelines aims to bring transparency and authenticity to published medical research.
Copyediting a process of checking the content of the manuscript. Copyediting is done by an experienced copyeditor. The function of a copyeditor is to check the grammatical errors, spelling mistakes, syntax, punctuation, and factual errors in the manuscript.
https://www.cognibrain.com/importance-of-copyediting-in-manuscripts/
Let’s learn those secrets from the renowned researchers who give you 7 top tips to publish your research.
https://www.cognibrain.com/steps-to-overcome-challenges-in-manuscript-publishing/
Scientific publications have a significant impact on the overall healthcare system. They are the source for in-depth, comprehensive, and up-to-date information. The doctors and other healthcare professionals find scientific publications as a support to their healthcare practice.
https://www.cognibrain.com/impact-of-scientific-publications-on-public-health/
Importance of Scientific Writing and Publishing for RadiologistsCognibrain Healthcare
The scientific writing by the radiologists serves a lot of purposes. Not only they are sharing their knowledge with their counterparts, but the scientific publication also helps to excel in their academic and professional career.
https://www.cognibrain.com/importance-of-scientific-writing-and-publishing-for-radiologists/
Scientific publications have a significant impact on the overall healthcare system. They are the source for in-depth, comprehensive, and up-to-date information.
https://www.cognibrain.com/impact-of-scientific-publications-on-public-health/
Evidence-based medicine is the system of practicing medicine in such a way that it results in improving outcomes and reduces the overall healthcare cost.
https://www.cognibrain.com/importance-of-evidence-based-medicine-on-research-and-practice/
Publishing an article in the journal adds to the academic performance of the researcher. Almost every researcher desire to publish their research articles in the reputed journal to ensure that it reaches maximum readers.
https://www.cognibrain.com/criteria-for-selecting-journal-for-publication/
The document discusses criteria for selecting the best journal to publish research manuscripts. Key criteria include the journal's impact factor, peer review process, author rights policies, business model, reputation, indexing in databases, scope, ethics guidelines, instructions for authors, and editorial board. Considering these factors will help researchers choose a journal that is a good fit for their research and increases the visibility and reach of their published work.
Every scientific paper is built upon previous research. Authors refer to the previous studies to find their topic of research and also to write their own medical manuscript. You must give credit to this previous research through citations and references.
https://www.cognibrain.com/how-to-write-references-in-the-medical-manuscript-quickly-and-easily/
Fit to Fly PCR Covid Testing at our Clinic Near YouNX Healthcare
A Fit-to-Fly PCR Test is a crucial service for travelers needing to meet the entry requirements of various countries or airlines. This test involves a polymerase chain reaction (PCR) test for COVID-19, which is considered the gold standard for detecting active infections. At our travel clinic in Leeds, we offer fast and reliable Fit to Fly PCR testing, providing you with an official certificate verifying your negative COVID-19 status. Our process is designed for convenience and accuracy, with quick turnaround times to ensure you receive your results and certificate in time for your departure. Trust our professional and experienced medical team to help you travel safely and compliantly, giving you peace of mind for your journey.www.nxhealthcare.co.uk
R3 Stem Cell Therapy: A New Hope for Women with Ovarian FailureR3 Stem Cell
Discover the groundbreaking advancements in stem cell therapy by R3 Stem Cell, offering new hope for women with ovarian failure. This innovative treatment aims to restore ovarian function, improve fertility, and enhance overall well-being, revolutionizing reproductive health for women worldwide.
The facial nerve, also known as cranial nerve VII, is one of the 12 cranial nerves originating from the brain. It's a mixed nerve, meaning it contains both sensory and motor fibres, and it plays a crucial role in controlling various facial muscles, as well as conveying sensory information from the taste buds on the anterior two-thirds of the tongue.
As Mumbai's premier kidney transplant and donation center, L H Hiranandani Hospital Powai is not just a medical facility; it's a beacon of hope where cutting-edge science meets compassionate care, transforming lives and redefining the standards of kidney health in India.
CHAPTER 1 SEMESTER V COMMUNICATION TECHNIQUES FOR CHILDREN.pdfSachin Sharma
Here are some key objectives of communication with children:
Build Trust and Security:
Establish a safe and supportive environment where children feel comfortable expressing themselves.
Encourage Expression:
Enable children to articulate their thoughts, feelings, and experiences.
Promote Emotional Understanding:
Help children identify and understand their own emotions and the emotions of others.
Enhance Listening Skills:
Develop children’s ability to listen attentively and respond appropriately.
Foster Positive Relationships:
Strengthen the bond between children and caregivers, peers, and other adults.
Support Learning and Development:
Aid cognitive and language development through engaging and meaningful conversations.
Teach Social Skills:
Encourage polite, respectful, and empathetic interactions with others.
Resolve Conflicts:
Provide tools and guidance for children to handle disagreements constructively.
Encourage Independence:
Support children in making decisions and solving problems on their own.
Provide Reassurance and Comfort:
Offer comfort and understanding during times of distress or uncertainty.
Reinforce Positive Behavior:
Acknowledge and encourage positive actions and behaviors.
Guide and Educate:
Offer clear instructions and explanations to help children understand expectations and learn new concepts.
By focusing on these objectives, communication with children can be both effective and nurturing, supporting their overall growth and well-being.
End-tidal carbon dioxide (ETCO2) is the level of carbon dioxide that is released at the end of an exhaled breath. ETCO2 levels reflect the adequacy with which carbon dioxide (CO2) is carried in the blood back to the lungs and exhaled.
Non-invasive methods for ETCO2 measurement include capnometry and capnography. Capnometry provides a numerical value for ETCO2. In contrast, capnography delivers a more comprehensive measurement that is displayed in both graphical (waveform) and numerical form.
Sidestream devices can monitor both intubated and non-intubated patients, while mainstream devices are most often limited to intubated patients.
NURSING MANAGEMENT OF PATIENT WITH EMPHYSEMA .PPTblessyjannu21
Prepared by Prof. BLESSY THOMAS, VICE PRINCIPAL, FNCON, SPN.
Emphysema is a disease condition of respiratory system.
Emphysema is an abnormal permanent enlargement of the air spaces distal to terminal bronchioles, accompanied by destruction of their walls and without obvious fibrosis.
Emphysema of lung is defined as hyper inflation of the lung ais spaces due to obstruction of non respiratory bronchioles as due to loss of elasticity of alveoli.
It is a type of chronic obstructive
pulmonary disease.
It is a progressive disease of lungs.
VEDANTA AIR AMBULANCE SERVICES IN REWA AT A COST-EFFECTIVE PRICE.pdfVedanta A
Air Ambulance Services In Rewa works in close coordination with ground-based emergency services, including local Emergency Medical Services, fire departments, and law enforcement agencies.
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This particular slides consist of- what is Pneumothorax,what are it's causes and it's effect on body, risk factors, symptoms,complications, diagnosis and role of physiotherapy in it.
This slide is very helpful for physiotherapy students and also for other medical and healthcare students.
Here is a summary of Pneumothorax:
Pneumothorax, also known as a collapsed lung, is a condition that occurs when air leaks into the space between the lung and chest wall. This air buildup puts pressure on the lung, preventing it from expanding fully when you breathe. A pneumothorax can cause a complete or partial collapse of the lung.
3. He is the person who writes
different types of high-quality
scientific documents that meet all
the regulatory requirements
4. Types of documents written by
medical writer
• Research proposals
• Investigator brochures
• Informed consent documents
• Clinical study reports
• Clinical trial protocols
• Package inserts
• Patient information leaflets
7. Knowledge of scientific domain
• Knowledge of different therapeutic areas
• Knowledge of regulatory guidelines
• Knowledge of statistics
8. Understanding of target audience
• Audience like regulatory
authorities, scientists, health
professionals, and the public
• Ability to write according to their
need
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9. Writing skills
• Accuracy in data interpretation and presentation
• Command over his language
• Ensures correct grammar, sentence structure, and
style
• Pays attention to detail and proofreads his content
11. Stays updated
• Stays abreast of new discoveries and
innovations
• Constantly learns new ideas
• Constantly improves his skills
• Learns and trains himself in new skill set
12. Clarity in presence
• Understands the objective of his project
• Can organize ideas precisely
• Represents information in clear and precise
manner
13. Excellent search strategy
Should have well-planned strategy for searching:
• Keywords
• Credible research articles for reference
14. Unbiased
• Reviews the research content in unbiased
manner
• Correctly interprets the results
• Truthfully identifies any limitations in research
content
15. Interpersonal skills
• Truthful in his dealings with the client
• Good listening skills
• Problem-solving skills
• Discussions and negotiating skills
• Decision-making skills
16. Project Management
• Highly active and organized
• Respects the deadlines
• Driven by quality of content
• Ready to accept responsibilities