Aakansha S. Profile

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$20 USD / hour

hyderabad,

india

$20 USD / hour

It's currently 7:14 PM here

Joined August 24, 2018

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Aakansha S.

@Aakanshasingh89

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(0 reviews)

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$20 USD / hour

hyderabad,

india

$20 USD / hour

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Scientific/Medical/Academic writer/Editor

A medical/scientific writer by profession with 4 years experience into academic research and medical writing. Writing and quality reviewer for reports for regulatory submissions and journals related to pharmaceuticals and cosmetics.

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Portfolio

The impact of cell culture technology has been immense in the field of research and pharmaceutical
sciences. Suitable environmental conditions are paramount need in order to maintain the cell line in an in-vitro
condition. Since the biological processes are highly susceptible to acid-base chemistry, variations among the factors
will have a severe effect on cellular integrity that often leads to hypercapnia and senescence of the cells. pH regulation
in the cell culture environment is a fundamental biological phenomenon of great significance for the growth and
metabolism of cells. This review focuses on the implications of the two critical factors carbon dioxide (CO2), pH, and
their correlated effects in the mammalian culture system. Bicarbonate buffer plays a vital role in maintaining
homeostasis as dissolved CO2 hydration occurs in HCO3⁻ and H+ equilibriums. If pH is not controlled, inhibition of
CO2 causes acidification in the medium. In contrast, if pH is not regulated by integrating

Implications of Carbon Dioxide in cell culture systems

6925827

Loading sd-rxRNAi into Tumors: Are We Getting Close with TGF

Implications of Carbon Dioxide in cell culture systems

6925827

Loading sd-rxRNAi into Tumors: Are We Getting Close with TGF

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Experience

Amazon

Nov 2019 - Jun 2020 (7 months, 1 day)

• Prepare, review and update the dangerous goods guidelines basis GHS and IATA. • Knowledge of consumer product compliance processes and regulations. • Experience in regulatory compliance management with government agencies. • Report violations of rules, regulations, policies, and procedures by evaluating or recommending the initiation of investigative and corrective procedures. • Classify products based on dangerous goods regulations.

Clarivate Analytics

Dec 2018 - Dec 2019 (1 year)

 Prepare, review, and revise publications and presentations for peer-reviewed journals and major conferences pertaining to the development of investigational medications, and.  Clinical, preclinical and drug development phase molecules.  Registering and updating radiopharmaceutical and radio diagnostic drug records in cortellis. Key areas: Drug discovery phase molecules, preclinical, clinical endpoints, gene therapy, immuno-oncology, stem cell therapy

Freyr Software Solutions

Aug 2017 - Nov 2018 (1 year, 3 months)

CLINICAL: Manage the writing, editing and reviewing of diverse regulatory & clinical documents including • clinical study reports, • study protocols, • investigator brochures, • informed consent forms, • clinical data summaries Non-clinical Drafting of Module 2 Common Technical Documents like Non-Clinical Overview (Module 2.4) and supporting IND projects based on FDA guidance for fixed dose combinations, Non-clinical summary (Module 2.6) and supporting IND projects.

Education

Masters in Pharmaceutical Chemistry

Swami Ramanand Teerth Marathwada University,

India

2010 - 2012

(2 years)

Qualifications

NIDA Clinical Trials Network

2020

Certificate of completion on “GOOD CLINICAL PRACTICE” via NIDA Clinical Trials Network. Course Completion Date: 27 April 2020; CTN Expiration Date: 27 April 2023.

Publications

Current Alarming Status, Strategies and Drug Development Pipeline for Tuberculosis

THE INTERNATIONAL RESEARCH JOURNAL “INTERNATIONAL RESEACHERS

This article intends to focus the current trends and new pipeline drug development including the new drug targets and the novel promising compounds under clinical trials.

Loading sd-rxRNAi into Tumors: Are We Getting Close with TGF-β1 Targeting?

Acta Scientific Pharmaceutical Sciences (ISSN: 2581-5423)

Adoptive cell therapies (ACT) that redirect T cells to specifically target cancer using genetically engineered T cell receptor or chimeric antigen receptor T cells are emerging forms of immunotherapy. Natural killer (NK) cells serve as a crucial first line of defense against tumors and can be activated rapidly to target and kill tumor cells without prior sensitization.