Executive Regulatory Affairs -- 2

Hi there, I have read your project entitled “Executive Regulatory Affairs” I am a Certified Chartered Accountant and a duly certified mentor of ACCA (UK). I have already done numerous projects of this sort. You can see my portfolio for this purpose https://www.freelancer.com/u/SIBTEHASSANBUTT I will deliver you the whole project whenever you need it. I will be happy to provide you with any revisions if you needed any. Let me do this job for you in a professional manner. After assigning me this project you need not worry about anything. looking forward to working with you. Experienced and competent finance professional with 5 years of experience, Knowledge and application of International Financial Reporting Standards (IFRS) and International Standards on Auditing, Knowledge of Corporate laws and Procurement Rules, Sound analytical and problem-solving skills, internal controls, Budgeting, Financial Reporting, Financial Modelling, Accounting Software, ERP, MS Excel, MS Word. My specialities are: -Payable & Receivables -Financial Data Entry -Finance, Management Accounting, Auditing & Bookkeeping, Accounting, -Financial Statements. -MIS, Budgeting, Forecasting & Variance Analysis. -Payroll -Audit of books of accounts. -Taxes -Reconciliations including banks, vendor, suppliers, financials. -Fixed Assets accounting & preparation of the register, calculation of depreciation aa Thanks. Member ACCA (UK), ACA (UK) finalist

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Hi, I have gone through your Job Description which suiting me I can fulfill your tasks on time. as I have an Experience in Regulatory affairs filings Dossier Submission for Asean,Africa, GCC, & Country Requirement dossiers, CTD, ACTD, I have required experience into the Regulatory affairs and I can Co-ordinate with the cross-functional teams QA, QC,R&D, Production for Documents to Compile in Dossier, BMR, BPR, MFR, COAS, Validation reports, Stability Reports, Packing requirements, Labelling and any other requirements.

Hello, I understand your requirement and having a rich experience of 7 years in the field of dug regulatory affairs for all dosage form. I can compile ctd, actd dossier in 1 day only if the doocuments are availble. If documents are not availble then the task may take 3 to 4 days.. Coordination with the different departments for collecting the data, review and compilation was included in my job profile.. The work will be done with higher accuracy considering the current guidlines and updated versions of pharmacopoeia.

I have very well knowledge and experience on non-clinical as well as clinical studies. I also have knowledge on ich guidelines gcp, glp, and gmp. I am well aware of regulatory submissions and dossier preparations. I can accomplish the work within stipulated time without any errors.