MedArk CRO

MedArk CRO full service clinical research organisation

  Mubarak to all   all over the world🌍.🎁Eid Mubarak to our  .🎉Eid   to MedArk CRO family.😍May all your upcoming days ful...
04/06/2025

Mubarak to all all over the world🌍.
🎁Eid Mubarak to our .
🎉Eid to MedArk CRO family.
😍May all your upcoming days full of happiness🌟, joy , love🌹 and .
www.medarkcro.com

🌟Once a   has passed preclinical research, it can proceed to   trials. These are studies that involve testing the drug o...
07/05/2025

🌟Once a has passed preclinical research, it can proceed to trials.
These are studies that involve testing the drug on human subjects.
🔥The aim of clinical trials is to assess the drug’s and in humans, as well as to determine the optimal .

🚀Clinical trials are a critical step in the , as they provide the evidence needed to demonstrate that a drug is safe and effective for its intended use.
Without this evidence, the drug would not be approved for sale.

💡Clinical trials are typically conducted in several , each with its own specific objectives and requirements.

🥇Contact the MedArk CRO team to know how they accelerate your clinical trials.
www.medarkcro.com

  is defined as an incident which deviates from the   protocol or   or expected conduct of the trial.  :The majority of ...
03/05/2025

is defined as an incident which deviates from the protocol or or expected conduct of the trial.
:
The majority of these deviations do not impact participants' or compromise the integrity of study data, and would be classified as minor.
:
deviations impact participants' or compromise the integrity of study data.

team in collaboration with the are playing vital roles in preventing/reduce deviations.

MedArk CRO team includes well trained and in addition to experienced who are capable of getting the most effective aligned with .

Contact our team for more details
www.medarkcro.com

💡An   trail is a secure, time-stamped record that   all changes made to electronic data throughout its lifecycle. 💡It pr...
15/04/2025

💡An trail is a secure, time-stamped record that all changes made to electronic data throughout its lifecycle.

💡It provides an unalterable log of who accessed or modified the , when it happened, and what changes were made.

💡Audit trails in clinical research serve as a “paper trail” for , including case report forms (eCRFs), laboratory results, and other study-related .

💡They that every action taken within a is documented and traceable, promoting and accountability.

🚀For your needs, we offer integrated clinical trial management services, including site management, management and monitoring.

🥇MedArk CRO is a full service CRO, you across every stage in the clinical journey.

🌟Speak to our to find out more about how we can help you.

www.medarkcro.com

💡Risk based monitoring (RBM) is used in     to assess the risks involved with the clinical study. 💡This assesses the ris...
09/04/2025

💡Risk based monitoring (RBM) is used in to assess the risks involved with the clinical study.
💡This assesses the risks to investigation quality, human subjects, data integrity, as well as lower-impact risks that are less likely to occur.

is a critical part of clinical , and is normally used to determine which type of monitoring is the most appropriate for the study.

🚀The risk-based monitoring process works by:

💡Identifying any potential
Designing a clinical monitoring plan
💡Adjusting the monitoring methodology where necessary
Risks are monitored in a number of ways, often through a combination of the types outlined in this article; on-site, remote and centralised methodologies.

🚀This mixed methods approach can help provide a more comprehensive overview of the trial, in turn, helping identify potential risks to and .

For your clinical development needs, MedArk CRO offers integrated clinical trial management services, including site management and monitoring.
We are a full service CRO, supporting you across every stage in the clinical journey.
Speak to our team to find out more about how we can help you.
www.medarkcro.com

https://www.linkedin.com/company/medark/

MedArk CRO is wishing a happy Eid 🎉 for all Muslims.Eid Mubarak 📿 to all our partners🥇, our team 💪and their families♥️.w...
28/03/2025

MedArk CRO is wishing a happy Eid 🎉 for all Muslims.
Eid Mubarak 📿 to all our partners🥇, our team 💪and their families♥️.

www.medarkcro.com

💡  (RWE) has become a transformative tool in clinical research worldwide. 💡  is clinical evidence regarding a medical pr...
25/03/2025

💡 (RWE) has become a transformative tool in clinical research worldwide.

💡 is clinical evidence regarding a medical product’s safety and efficacy, generated using Real-World Data (RWD) derived from routine healthcare delivery.

💡This data is collected from diverse sources such as electronic health records (EHRs), registries, insurance claims, mobile health applications, wearable devices, and patient-generated information.

💡In a region with diverse populations and unique healthcare challenges, is providing critical insights that complement traditional clinical trial , making it a valuable resource for optimizing trial designs, research quality, and patient outcomes.

MedArk CRO team as a pioneer in providing research services, is ready to accelerate your studies across GCC and MENA regions.

contact us for more details:
www.medarkcro.com

   's   (IWD) 2025 will be celebrated globally on Saturday, March 8, under the campaign theme “ ." 🚀This campaign theme ...
07/03/2025

's (IWD) 2025 will be celebrated globally on Saturday, March 8, under the campaign theme “ ."

🚀This campaign theme emphasises the urgent need to take decisive steps toward achieving gender , the slow pace of progress, and women and girls worldwide.

MedArk CRO is proud to be a CRO which is fully founded and managed by super💪, multinational and experts women.

♥️Happy international women's day

Clinical Trials For All


www.medarkcro.com

    play a vital role in ensuring accountability and transparency in   research. By providing: ♟️a comprehensive record ...
05/03/2025

play a vital role in ensuring accountability and transparency in research.
By providing:
♟️a comprehensive record of all interactions with electronic data.
♟️they support regulatory compliance
♟️protect data integrity
♟️promote ethical conduct.

🚀As the industry continues to evolve, embracing advanced technologies and adhering to best practices will be essential for leveraging audit trails to their full potential.

At , we understand the significance of audit trails in delivering high-quality, compliant clinical trials.
💡Our team of specializes in integrating solutions to meet your research needs.

👍 Contact us today to learn more about how we can assist you in achieving seamless compliance and operational excellence.

www.medarkcro.com

https://www.linkedin.com/company/medark/

https://www.facebook.com/share/151DGvCRjW/


Clinical Trials For All

تهنئه قلبيه من فريق عمل MedArk CRO بحلول شهر رمضان المبارك.رمضان مبارك على الأمه الاسلاميه و على شركاء نجاحنا و عملائنا....
27/02/2025

تهنئه قلبيه من فريق عمل MedArk CRO بحلول شهر رمضان المبارك.
رمضان مبارك على الأمه الاسلاميه و على شركاء نجاحنا و عملائنا.
كل عام و انتم بألف خير.
كل عام و فريق عملنا بألف خير.
أعاده الله علينا و عليكم و على الأمه الاسلاميه بالخير و اليمن و البركات.

Heartfelt congratulations from the MedArk CRO team on the occasion of the holy month of Ramadan.
Ramadan Mubarak to the Islamic nation and to our success partners, stakeholders and customers.

www.medarkcro.com

.
Clinical Trials For All

بمناسبه  #يوم التاسيس  #السعودي تتقدم MedArk CRO  بخالص التهاني لكل عملائها و شركاء نجاحها داخل المملكه.كل عام و المملكه...
22/02/2025

بمناسبه #يوم التاسيس #السعودي تتقدم MedArk CRO بخالص التهاني لكل عملائها و شركاء نجاحها داخل المملكه.
كل عام و المملكه و ملكها و ولي عهدها و شعبها بألف خير و ازدهار.


On the occasion of the Saudi Founding Day, MedArk CRO extends its sincere congratulations to all its clients and partners for its success within the Kingdom.
Happy day to the Kingdom, its king, its crown prince and its people.

www.medarkcro.com

   ♟️Any unfavourable or unintended symptom or sign, including change in laboratory results, temporarily associated with...
21/02/2025


♟️Any unfavourable or unintended symptom or sign, including change in laboratory results, temporarily associated with an intervention during the conduct of a .
♟️ It does not matter whether this event is considered related or unrelated to this intervention.
♟️These events should be recorded in both the data (commonly medical notes) and the (CRF) or adverse event log.
♟️The trial should stipulate the necessary requirements for reporting.

To know more about services contact our team
www.medarkcro.com


MedArk CRO

Address

UAE
Sharjah

Alerts

Be the first to know and let us send you an email when MedArk CRO posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Share

Share on Facebook Share on Twitter Share on LinkedIn
Share on Pinterest Share on Reddit Share via Email
Share on WhatsApp Share on Instagram Share on Telegram