ONYX Education and Research

Dear Scientists, Researchers, and Academicians,

We at Zyirn Research Consultancy Services are industry experienced life science consultants offering our expertise at every stage of research and development processes.

We are happy to announce Webinar on :

Document Control In Good Laboratory Practices – Why and How?.

Webinar Date: July 25, Sunday

Webinar Time: 5:00 - 7:00 pm IST.

Registration Fee: Rs. 500 (For more than 5 participants we will give you discounted rates. Please connect with us on [email protected])

Pay via Google Pay: +91 9820310424

And PayU money link: https://pmny.in/fIaObjSdQqC0

Register Now: https://zyirn.com/registration/

Documentation and Record Keeping is pivotal part of Good Laboratory Practice and so is the control of these documents and records. Documents provide essential guidelines for the laboratory in the form of a quality manual, SOPs, reference material, study plans and experimental data records. They are required part of the laboratory quality standards. They reflect the laboratory's organization and quality management. Laboratories maintain documents and records to find information when it is needed.

In this webinar, learn why you need to control documents and what are the ways and means to do that. A complete guide to document control in Good Laboratory Practices.

Know about our services: https://zyirn.com/

Connect with us on LinkedIn: https://www.linkedin.com/company/zyirn-research-consultancy-services/

You are also requested to pass on this to your friends, colleagues, juniors and staff, who may be interested in this and can be benefitted from this.

Looking forward to see you in the webinar. Please revert back for any queries or clarification.

Best Regards,
Nimisha Sharma
Business Development Director
Zyirn Research Consultancy Services

W: www.zyirn.com
E: [email protected]
P: +1 4036047869
Connect on LinkedIn

Dear Scientist,

As global growth partners, We at Zyirn Research Consultancy Services (ZRCS) provide unique propositions delivering results at every stage of the life science research process to help academic researchers, scientists, and mid and large sized biotech, medical devices, agrochemical and pharmaceutical companies achieve their scientific goals faster.

We are happy to announce:

Free webinar on “Principles of GLP: The Primary Elements”

Date: June 13, Sunday

Time: 4.00 -5.30 PM IST

Speaker: Dr. Imran Khan

Register here: https://lnkd.in/gmbDRiM

By taking this webinar, you will know the principles of good laboratory practices (GLP) and its importance within a regulated laboratory environment. The benefits of GLP and how it leads to the creation of technically defendable scientific data, by which its quality, reliability and trustworthiness can be assured.

Do follow us on LinkedIn: https://bit.ly/3gnD2Aa

We look forward to your participation.

Thanks and best regards

Zyirn Research Consultancy Services

Online Training: “Repeat Dose Toxicity Studies” 23May2021 02:00 to 04:00 PM (IST)

Dear All,

Trichinopoly.i (https://trichinopolydotin.com/) is pleased to announce an online training program for students, freshers, study directors (SD), principal investigators (PI), study personnel (SP) and all candidates working in the field of pre-clinical contract research organizations (CROs), pharmaceutical companies, drug discovery partners, biotech companies, medical device companies, etc.

Trainer: Dr. M. Imran Khan (https://trichinopolydotin.com/dr-mohammed-imran-khan/) has more than 20 years of experience of working in the area of regulatory toxicology, safety assessment, and in vivo testing for the pharmaceuticals, agrochemicals, medical devices, etc. He has experience of submitting toxicity data to different regulatory authorities like DCGI, USFDA, CIB&RC, etc. following OECD, EU, ICH, Schedule Y and CIB guidelines. He has conducted many repeat dose toxicity studies by himself and has trained many Study Directors to conduct the repeat dose toxicity studies of varied durations successfully.

In the assessment and evaluation of the toxic characteristics of a chemical, the determination of toxicity by different routes using repeated doses may be carried out after initial information on toxicity has been obtained by acute toxicity testing, to investigate effects on a very broad variety of potential targets of toxicity. The repeat dose toxicity studies provide information on the possible health hazards likely to arise from repeated exposure over a defined period of time, including effects on the nervous, immune and endocrine systems, etc. These results are used for hazard identification and risk assessment for such chemicals. In this presentation we are going to see why these repeat dose studies are important and mandatory for registration purposes and what are the requirements of different regulatory bodies. We will also cover some of the important practical points for proper conduct of these studies, for best results.

All the Seniors /Group Leaders /Managers /Team Leaders are requested to forward it to their concerned team members and nominate more and more staff from their companies /organizations /institutes for this.

Soft copy Attendance /Participation Certificate will be provided to all the registered participants.

Please find attached the flyer of the training program with all the details.

Also find below the link for registration:
https://trichinopolydotin.com/registration-form/

Looking forward to seeing you all for this program.

NOTES:

1. Please share your payment details (screen shot or payment receipt) on WhatsApp (9820310424 /6380376573) and on email ([email protected]; and [email protected]), so that we don't miss to send you the link and invite.

2. The meeting invite and link to join the meeting will be shared with individual participants only one day in advance i.e. on Saturday 22May2021.

3. In case you do not get invite and link by end of 22May21, please get in touch with us on above details.

4. The presentation of the training program (PDF) will be shared with all registered participants within 1-2 days after the training.

5. The soft copy participation certificate may take a week's time for sharing with all. Though we try to give it within 4 days after the training session.

Thanks and best regards

Dr. M. Imran Khan, M.V.Sc., PGDMM
Director Operations (Consultant),
TRICHINOPOLY.I
Consultant,
GReAT Consultancy Services
(GLP, Regulatory, Animal Facility, Toxicology)
Mumbai, India
Mobile: +91 - 98 2031 0424
Email: [email protected]

Hi.
Good morning everyone.
A very happy Gudi Padwa (Maharashtra New Year),
A very happy Ugadi (Andhra and Telangana New Year),
A very happy new year to all states celebrating New Year Today.
May this new year bring new joy, happiness, prosperity, health, wealth and peace in everyone's life.
God bless all.
🎊🎊🎉🎉🎇🎇🎆🎆🎊🎊🎉🎉

Dear All,

Qualification and Validation of equipments is very important topic in GLP and GXP.
Last day to register for 04Apr2021 training program.

Please find below the link for registration:

https://trichinopolydotin.com/registration-form/

Please forward it to all who can benefit from this.

Thanks and best regards

Dr. Imran Khan

Dear All,
I am very happy to inform you all again that, I have successfully completed the 15 Credit International Certified Career Coach - Foundation Program organized by Mindler in association with Career Development Alliance (USA) on 26th and 27th Mar2021.

This is my second certificate of Level-1 Foundation Program.
Looking forward to the Advanced and Masters Programs soon.

Thank you Mindler and thank you CDA (USA).
Thank you all.
God bless you all.

Online Training:
"Qualification and Validation of Equipment under GLP"
04Apr2021 02:00-04:00 PM (IST)

Dear All,

Trichinopoly.i (https://trichinopolydotin.com/) is pleased to announce an online GLP training program for students, freshers, study directors (SD), principal investigators (PI), study personnel (SP) and all GLP personnel working in the field of pre-clinical contract research organizations (CROs), pharmaceutical companies, drug discovery partners, biotech companies, medical device companies, etc.

Trainer: Dr. M. Imran Khan (https://trichinopolydotin.com/dr-mohammed-imran-khan/) has more than 20 years of experience of working under GLP, implementing the GLP in organizations and getting the GLP Certification from Netherland, Swiss and Indian Authorities, and successfully running the GLP complaint organizations. During this tenure he has worked in the area of regulatory toxicology, safety assessment, and in vivo testing for the pharmaceuticals, agrochemicals, medical devices, etc.

To perform a study properly, adequate equipment suitable for its intended use i.e. fir for purpose and fit for use, should be available. Suitability of equipment can only be assessed by consideration of the performance of the equipment i.e. formal qualification to demonstrate that it is fit for its intended use. The formal qualification and validation of equipment covers DQ, IQ, OQ and PQ of the equipment along with proper and regular calibration and maintenance to ensure accurate performance. In this training program we will see in details different aspects of qualification, validation, calibration and maintenance of the equipment used in GLP for conducting studies.

All the Seniors /Group Leaders /Managers /Team Leaders are requested to forward it to their concerned team members and nominate more and more staff from their companies /organizations /institutes for this program.

Soft copy Attendance /Participation Certificate will be provided to all the registered participants.

Please find attached the flyer of the training program with all the details.

Also find below the link for registration:

https://trichinopolydotin.com/registration-form/

Looking forward to seeing you all for this program.

NOTES:
1. Please share your payment details (screen shot or payment receipt) on WhatsApp (9820310424 /6380376573) and on email ([email protected]; and [email protected]), so that we don't miss to send you the link and invite.

2. The meeting invite and link to join the meeting will be shared with individual participants only one day in advance i.e. on Saturday 03Apr2021.

3. In case you do not get invite and link by end of 03Apr21, please get in touch with us on above details.

4. The presentation of the training program (PDF) will be shared with all registered participants within 1-2 days after the training.

5. The soft copy participation certificate may take a week's time for sharing with all. Though we try to give it within 4 days after the training session.

Thanks and best regards

Dr. M. Imran Khan, M.V.Sc., PGDMM
Director Operations (Consultant),
TRICHINOPOLY.I

Consultant,
GReAT Consultancy Services
(GLP, Regulatory, Animal Facility, Toxicology)
Mumbai, India
Mobile: +91 - 98 2031 0424 Email: [email protected]

Dear All,

Successfully completed another Online Training program, "Multi-site Studies under GLP" on 14Mar2021.

This was my 7th training program in as many months.

I sincerely thank all the participants for participating and taking part in extremely beneficial question answer session towards the end.
The feedback received from participants is overwhelming and heart touching.

A sincere and heart felt gratitude to all of the participants till now.

I am really very much supported and encouraged to plan such sessions in future too and I promise you all, I will be doing it on regular basis.

Thank you one and all.
Have a safe and great time ahead.
Wishing you all the success in all of your endeavours.
God bless you all.

Dr. Imran Khan
9820310424
[email protected]

Received the Certificate for successfully completing Department of Science and Technology (DST) Sponsored fortnight e-training (Online) under Faculty Development Program (FDP) on " Entrepreneurship in Livestock and Veterinary Science" during 09-22 Feb 2021. Hosting Institute: ICAR-NRC on Meat, Hyderabad

Online Training:
Multi-site Studies under GLP
14Mar2021_02:00-04:00 PM (IST)

Dear All,

Trichinopoly.i (https://trichinopolydotin.com/) is pleased to announce an online GLP training program for students, freshers, study directors (SD), principal investigators (PI), study personnel (SP) and all GLP personnel working in the field of pre-clinical contract research organizations (CROs), pharmaceutical companies, drug discovery partners, biotech companies, medical device companies, etc.

Trainer:
Dr. M. Imran Khan (https://trichinopolydotin.com/dr-mohammed-imran-khan/) has more than 20 years of experience of working under GLP, implementing the GLP in organizations and getting the GLP Certification from Netherland, Swiss and Indian Authorities, and successfully running the GLP complaint organizations. During this tenure he has worked in the area of regulatory toxicology, safety assessment, and in vivo testing for the pharmaceuticals, agrochemicals, medical devices, etc.

A multi-site study means any study that has phases conducted at more than one site. A study can be a “multi-site” study for a variety of reasons. It is becoming increasingly common for non-clinical health and environmental safety studies to be conducted at more than one site. In this training session we will learn and understand different GLP related issues that are involved in the planning, performance, monitoring, recording, reporting and archiving of multi-site studies i.e. complete organization, management and control of the Multi-site studies.

All the Seniors /Group Leaders /Managers /Team Leaders are requested to forward it to their concerned team members and nominate more and more staff from their companies /organizations /institutes for this program.

Soft copy Attendance /Participation Certificate will be provided to all the registered participants.

Please find attached the flyer of the training program with all the details.

Also find below the link for registration:
https://trichinopolydotin.com/registration-form/

Looking forward to seeing you all for this program.

NOTES:
1. Please share your payment details (screen shot or payment receipt) on WhatsApp (9820310424 /6380376573) and on email ([email protected]; and [email protected]), so that we don't miss to send you the link and invite.
2. The meeting invite and link to join the meeting will be shared with individual participants only one day in advance i.e. on Saturday 13Mar2021.
3. In case you do not get invite and link by end of 13Mar21, please get in touch with us on above details.
4. The presentation of the training program (PDF) will be shared with all registered participants within 1-2 days after the training.
5. The soft copy participation certificate may take a week's time for sharing with all. Though we try to give it within 4 days after the training session.

Thanks and best regards

Dr. M. Imran Khan, M.V.Sc., PGDMM
Director Operations (Consultant),
TRICHINOPOLY.I
Consultant,
GReAT Consultancy Services
(GLP, Regulatory, Animal Facility, Toxicology)
Mumbai, India
Mobile: +91 - 98 2031 0424 Email: [email protected]