You will get perfect consultancy in writing Pharmaceutical SOPs
You will get perfect consultancy in writing Pharmaceutical SOPs
Project details
Are you looking for Pharmaceutical COntent? Or do you need to scale your newly GMP-complained Industry by having content related to WHO guidelines? If yes, then you have come to the right profile. I'm Awais, having professional experience of 15 years in the pharmaceutical industry.
I can write Production, Quality & Validation related SOPs, Batch Manufacturing & packaging Records/protocol, Quality Policies, Test Procedures, APR, GMP-related documents, pharmaceutical Production Planning, SAP Material Master SOPs as per International Standards of WHO guidelines, FDA and USP/BP.
Following are some of the services that I can develop content for you:
1-ISO-based documents (QMS and EMS).
2-FDA-based Documents (GMP).
3-ICH Guidelines
4-WHO-based guidelines.
Besides this, I am providing an unlimited number of revisions and proofreading services when needed.
If you have any queries related don't hesitate to contact me.
I can write Production, Quality & Validation related SOPs, Batch Manufacturing & packaging Records/protocol, Quality Policies, Test Procedures, APR, GMP-related documents, pharmaceutical Production Planning, SAP Material Master SOPs as per International Standards of WHO guidelines, FDA and USP/BP.
Following are some of the services that I can develop content for you:
1-ISO-based documents (QMS and EMS).
2-FDA-based Documents (GMP).
3-ICH Guidelines
4-WHO-based guidelines.
Besides this, I am providing an unlimited number of revisions and proofreading services when needed.
If you have any queries related don't hesitate to contact me.
Service Type
SummaryLanguage
EnglishWhat's included
| Service Tiers |
Starter
$5
|
Standard
$10
|
Advanced
$20
|
|---|---|---|---|
| Delivery Time | 1 day | 3 days | 5 days |
Number of Revisions | Unlimited | 3 | 3 |
Additional Research | - | - | - |
References & Citations | - | - | - |
About Awais
Pharmaceutical Industry | Regulatory | Content Writing | Resume
Karachi, Pakistan - 2:56 pm local time
🏅I have more than 15 years of experience in the field of Pharmaceutical Industry with top notch firms with successful track in career. 🌟🌟🌟🌟🌟
✨My LinkedIn Page has 3 K+ Followers, and my Content has reached 1.5 K+ Impressions in 15 days
🟡I will guide and assist you with WHO Compliance /Pharmaceutical Quality System (PQS) & GMP PICs Audit | Dosage forms Manufacturing | Validation [Process Validation & Computer System Validation CSV]
I’ve spent the last 10 years in learning everything there is to know about the Pharmaceutical industry, from FDA Regulatory Affairs; eCTD / CMC, and Good Manufacturing Practice & Quality Management Systems; To Project Management and Processes Improvement and Deliver Operational Excellence.
Being a health care professional with background experience in Quality Assurance, FDA and WHO guidelines SOPs regarding Pharmaceutical field with multi level tasking personnel. Handled RCA and investigations to provide maximum results using statistical tools.
Currently i am Lead Manager Production in my role and registered licenced holder from Pharmacy Council, where I’m responsible for Ensuring compliance with GxP and regulatory requirements in regulated Firms producing Sterile /Non-Sterile settings such as pharmaceuticals as per WHO Quality, ISO Standards 9001:2015, and 21 CFR part 11.
I am self-motivated, a Continuous Learner, good decision maker, and able to work independently as well as with a team, I used to use work professional skills in solving problems, analyzing data, and implementing process improvement and Re-Engineering through Risk Assessment based thinking, and techniques, encouraging Teamwork, and Communication between the process owners.
I will be glad to provide support to you and your team in the development,selection of dosage form, technology used for Manufacturing operations (Sterile and non-sterile) and Implementation of cGMP, quality processes & activities, and ensure readiness for FDA audit.
Furthermore, I’m happy to connect with Pharmaceutical Industry professionals.
I look forward to hearing from you!
Best Regards,
Awais Hussain
Steps for completing your project
After purchasing the project, send requirements so Awais can start the project.
Delivery time starts when Awais receives requirements from you.
Awais works on your project following the steps below.
Revisions may occur after the delivery date.
Content Medical & Pharmaceutical