Ziva DRA

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Ziva DRA

Comprehensive regulatory & compliance service provider in Bangladesh for Medical devices, IVDs, Pharmaceuticals & Cosmetics industries.

Ziva D.R.A is a comprehensive Regulatory service provider in Bangladesh. We provide regulatory services for Pharmaceuticals, Medical devices, Cosmetics and Foods industry. With a team of experts and a commitment to excellence, we empower businesses to thrive by simplifying regulatory processes and ensuring compliance. We provide services in Bangladesh market-
1. Medical Device Registration in Bangladesh
2. API Registration/ Source validation in Bangladesh
3. Cosmetics Registration in Bangladesh
4. IVDs registration in Bangladesh
5. HR payrolls service in Bangladesh
6. Headhunting service in Bangladesh
7. Global Regulatory service
8. Contact research organisation (CRO) in Bangladesh
9. Company formation and regulatory compliance
10. VAT & TAX management service in Bangladesh

We are best regulatory service provider in Bangladesh in terms of our expertise and working experience. Contact us for your queries.

04/12/2025

Veterinary Medicine Registration in Bangladesh

02/12/2025

The Tax Registration Checklist You Wish You Had Sooner

01/12/2025

Let's be clear: in highly regulated industries, information is abundant, but insight is scarce. The critical bridge between the two is built through dedicated Regulatory Intelligence.

This goes beyond basic surveillance; it's the disciplined practice of gathering, analyzing, and communicating the implications of regulatory information to guide an organization's path forward.

Forget about drowning in daily alerts. The goal of modern Regulatory Intelligence is to provide decision-makers with clarity—enabling confident choices on everything from development pipelines and target markets to resource allocation and external engagement.

It empowers professionals to not only ensure compliance but also to identify opportunities within the evolving regulatory landscape.

The foundation is a robust process: continuous monitoring, impact analysis, and the integration of findings into business workflows. However, the true catalyst is the human element, the expertise to interpret nuances, forecast trends, and align intelligence with core business objectives.

How is your organization cultivating its Regulatory Intelligence capability? The quality of your regulatory insight directly influences the speed and security of your market journey.

28/11/2025

How to Set Up Your Liaison Office in Bangladesh: A Practical Roadmap

14/11/2025

Liaison office registration in Bangladesh

11/11/2025

Foreign company registration in Bangladesh

02/11/2025

Navigating the New Era of Cosmetics Registration in Bangladesh

Thinking of launching or importing cosmetic products in Bangladesh? The regulatory landscape has undergone a significant shift, and staying informed is key to a successful market entry.

The entire process for cosmetics registration in Bangladesh is now handled by the Directorate General of Drug Administration (DGDA), moving away from the BSTI. This change, formalized under the new Drug & Cosmetics Act 2023, means that everything from moisturizers to medicated skin creams requires proper approval from the DGDA.

Understanding the pathway for cosmetics registration in Bangladesh is your first step toward compliance. While the process is detailed, it can be navigated smoothly with the right preparation. Key steps typically involve:

Company registration with the Registrar of Joint Stock Companies (RJSC).

Securing an Import Registration Certificate (IRC) for importers.

Preparing a comprehensive product dossier including GMP, Certificate of Analysis (COA), safety data, and formulation details.

Why is this so critical? Simply put, a completed cosmetics registration in Bangladesh is your license to operate. Without it, you risk facing troubles at customs, market bans, and loss of trust with retailers and consumers. Compliance is no longer just a formality; it's a core component of your brand's credibility.

Currently, the DGDA processing timelines can be uncertain due to the newness of the regulations. However, planning for a 6–12 month process, depending on the completeness of your documentation, is a prudent approach. For products with therapeutic claims, such as anti-acne or anti-hair fall, expect a closer level of scrutiny from the authority.

My advice? Don't navigate this journey alone. Consider partnering with a regulatory consultant who specializes in the Bangladeshi market. They can help fast-track your application, from dossier preparation to final approvals, saving you valuable time and resources.

Interested in learning more about the specific documentation required for your product? Feel free to drop a comment or send me a direct message.

01/11/2025

Navigating the Landscape of Regulatory Affairs Jobs

The world of regulatory affairs jobs is more dynamic than ever. With a quick search showing thousands of open roles across the United States, from specialists in medical devices at major tech firms to directors shaping global strategy in pharma, the opportunity is vast.

But in such a competitive field, how do you stand out?

It’s not just about applying; it’s about being found. For professionals eyeing their next move in regulatory affairs jobs, the real game-changer is often a strategically optimized presence. Think of your profile not as a digital resume, but as a destination. It should be built not just with keywords, but with context.

This is where understanding modern search, AEO (Answer Engine Optimization), and traditional SEO becomes crucial. It’s the difference between being seen by recruiters and being overlooked.

From my experience, here are a few advanced levers to pull:

Go Beyond the Job Title in Your Headline: Your headline shouldn’t just state your current position. Weave in the specific domains, regulations, and product types you specialize in. This creates a rich keyword semantic field that aligns with how recruiters and hiring managers search.

Optimize Your 'About' Section for Intent: The first three lines of your summary are prime real estate. Use them to clearly state the problems you solve and the value you bring, incorporating the core terms a hiring manager would use to find a candidate for those regulatory affairs jobs you want.

Quantify Your Narrative in Experience: Instead of listing duties, frame your accomplishments around impact. For instance, "Led the FDA submission for a novel cardiac device, resulting in approval within 12 months" is far more powerful and searchable than "Responsible for regulatory submissions."

The landscape of regulatory affairs jobs is rich with potential. By shifting your approach from passive applicant to active, optimized candidate, you position yourself at the forefront of the search.

What has been your most effective strategy for visibility in the job market? Share your thoughts in the comments below.

28/10/2025

The Strategic Engine You're Likely Underused: Market Research

We throw around the term "market research" a lot. But how many of us treat it as the continuous strategic engine it is, rather than a one-time project?

The goal of true market research isn't just to collect data. It's to silence the internal guesswork and answer three critical questions with evidence: What is happening, why is it happening, and what should we do next?

Many organizations stop at the first stage. They see a dip in sales or a new competitor and react. Advanced practitioners use ongoing market research to predict the dip, understand the competitor's true threat level, and have a strategy in place before the trend becomes a crisis.

This is where qualitative insights meet quantitative data. It’s not enough to know that 30% of your users churned. You must know why. This requires a disciplined blend of data analytics (the "what") and deep, conversational customer interviews (the "why"). This synthesis is where the real gold is.

Your next product iteration, messaging pivot, or entry into a new segment should be a direct outcome of this rigorous market research process. It removes opinion from the decision-making table and replaces it with market intelligence.

How are you structuring your market research to be a proactive strategy, not a reactive report?

23/10/2025

Beyond the Data Stream: The Human Story in Bioanalytics

We often talk about bioanalytics in terms of throughput, sensitivity, and p-values. And rightly so. The precision of our LC-MS/MS systems and the power of our immunoassays are the bedrock of what we do.

But I was reminded this week that the most advanced bioanalytics are meaningless without a story.

We received a set of samples for a new oncology program. The data came in, clean chromatograms, perfect calibration curves. Statistically, it was a flawless run.

But when we integrated the pharmacokinetic data with the pharmacodynamic readouts from our clinical colleagues, a different narrative emerged. The numbers weren't just data points; they were a map. A map that showed us not just if the drug was present, but what it was doing.

This is where true, advanced bioanalytics earns its keep. It's the critical bridge between a compound's concentration in the blood and its biological effect on a patient. It’s the discipline that asks the "so what?" after the "how much?"

The next frontier in bioanalytics isn't just about faster or cheaper assays. It's about deeper integration. It's about weaving our quantitative data with genomic, proteomic, and digital health data to build a holistic picture of patient response. This integrated approach is how we move from simply monitoring drugs to truly understanding therapies.

The machines generate the data, but we, the scientists, uncover the story within it.

What are your thoughts on the evolving role of the bioanalytical scientist in this integrated landscape?

21/10/2025

Active Pharmaceutical Ingredients (API) Registration or Source Validation in Bangladesh

Exporting APIs to Bangladesh? Regulatory compliance is a mandatory step — and Ziva DRA is here to make the process smooth and efficient.

At Ziva DRA, we specialize in API registration and source validation services to help pharmaceutical companies meet all local regulatory requirements with confidence.

✅ Streamlined registration process
✅ Expert regulatory documentation support
✅ Hassle-free coordination with authorities

Let us help you ensure your APIs are fully compliant and ready for export to Bangladesh.

📞 Contact us today for consultation:
📱 +8801915536110
📧 zivadrabd@gmail.com
🌐 www.zivadra.com

20/10/2025

Consultant with our income tax practitioner for your tax return.

Address

Shantinagar
Dhaka
1217

Website

http://zivadra.com/

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