What can Zyirn do for you?
- Lab Design and Validation Services
- Quality Assessment / Quality Assurance
- Scientific Writing / Content Writing
- Regulatory Services
- Drug Discovery and Development
- Preclinical Toxicology
- Research Staffing and Training Services
What are Zyirn’s Core Values?
Do you provide free consultations?
How can I contribute to the Zyirn blog?
I am a consultant; how do I work with Zyirn? (Should we add this q? Yes)
Are there any fees to register as an expert /consultant on Zyirn?
How can I contact support?
How does the process work?
We have a time-tested system, wherein the CROs we collaborate with, allow our sponsors/clients to have physical visit to their facilities and offices and validate the facilities are indeed GLP complaint, adhering to all animal welfare measures as mandated by CPCSEA and AAALAC International or to any other international animal welfare and quality standards like ISO.
Due to time and cost limitations, it may not be always possible for the client or the Sponsor representative to visit the facility across the international borders. On behalf of our clients and sponsors, we audit the facilities or CROs to assess their compliance with GLP, GXP, ISO and animal welfare measures as per recommendations of their countries Animal Welfare Authorities / requirements.
We do not limit ourselves with facility audits only but hand hold the sponsor /clients in identifying the best suited, cost effective CROs /lab, identifying the studies required to be submitted to the authorities as per sponsor needs, placing the studies with the CROs and monitoring the whole project from beginning till the end. The critical aspects of the monitoring of such projects are reviewing the study plans or protocols, reviewing the raw data and progress of the project from time to time and reviewing of the draft reports before finalization, so that the project timelines are adhered with and also the report generated are of good quality and integrity with respect to the data so that the sponsor and regulatory authorities can accept the data.
We do understand that such projects are often long term engagements and can go on for months and even years depending on the project size and the duration of studies and thus involve significant investment on part of the sponsor /client, we always prefer to get into service agreements and confidentiality agreements with sponsor as well as CROs to safeguard scientific discoveries /inventions /intellectual properties of the clients.
On the longer term projects, our clients can complete their projects / studies with a significant discount (cost saving) than what a similar project would require if it were to be conducted in the Western laboratories.
Thus we offer a great win-win-win situation for all the parties. The Clients get the project completed with quality and integrity well within the project timelines in a cost effective efficient manner, the CROs get the consistent / repeat business from the satisfied clients and we get our pay-for-service charges and also the satisfaction of helping both the parties in achieving their goals and targets.
What areas do you specialize in?
- Pharmacology and drug discovery in therapeutic areas Diabetes, Obesity, Oncology, Inflammation, Infectious Diseases, Respiratory Diseases and CNS disorders
- Toxicology including pathology and histopathology
- Regulatory compliance reports
- Animal Welfare and Animal Facility compliance with governing bodies such as CPCSEA, AAALAC
The animal models for disease (disease models), safety pharmacology and animal breeding on conventional as well as transgenic animals are other areas of our expertise.
For more information on our services and detailed list of services within each broad head, please visit our services section and /or write to us on firstname.lastname@example.org
Will you sign a non-disclosure agreement?
Where are you located and how do you work with clients outside your local area?
Do you have references?
Is your service secure?
Who owns the IP of the project deliverables?
What is your billing policy?
We provide at least 2 weeks of time from generating the invoice to the clients for making the payment.
What is your cancelation policy?
What happens if I decide to cancel my contract?
What type of documents do you edit?
What kind of document formats can I send you?
Who does the editing?
How long will it take?
How much will it cost?
What is the turnaround time?
What is the typical process for an editing job?
- Client submits scientific manuscript/ document for editing
- Zyirn editors edit and deliver the document to client
- Client reviews file with edits & communicates with Zyirn
- If changes are required, Zyirn edits & delivers the document to client for submission
- Incase of manuscripts and regulatory compliance documents, the client submits the document to the journal / regulatory body respectively
- Client receives response from journal/ regulatory body
- If there are any recommendations, client submits changes to Zyirn under Edit Unlimited
- Zyirn will edit & deliver publication/ submission -ready documents to clients.
Accelerate your research goals, connect with us today for all your scientific writing needs. Contact us.
Do you offer discounts?
Will you guarantee my paper will be published?
Training - Individual and Enterprise solutions
How is your training different from other training providers?
What equipment do I need and how do I access my course?
Can I record the sessions?
Will I get a Certificate for the training?
What form of payments do you accept?
Do you offer volume discounts?
Do you offer content or topic customized courses?
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