Ziva DRA

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.

You've just seen a brilliantly creative interactive marketing campaign. It's personalized, engaging, and perfectly targe...
27/12/2025

You've just seen a brilliantly creative interactive marketing campaign. It's personalized, engaging, and perfectly targeted. My first thought? "That's a compliance minefield."

It’s true. The most innovative campaigns—from interactive investment calculators to AI-powered chatbots—often create the biggest headaches for IT compliance and legal teams. Every personalized web experience, especially in finance, brings risks around proper disclaimers, data handling, and the monumental task of archiving dynamic content for regulators. The creativity that captures your audience can also capture the attention of enforcement agencies.

The reality is that IT compliance can no longer be a siloed, rear-view-mirror function. It must be integrated, proactive, and pragmatic. Based on the evolving landscape, here are three actionable strategies to get ahead.

1. Govern Your Third-Party Digital Ecosystem. The biggest blind spot in 2025 is the gap between companies and their vendors, like marketing agencies. A pixel is added with a click, but is there a process for its review or removal? Your action item: Review every agency contract. Clearly define who owns the responsibility for data privacy compliance. Then, establish a regular audit cadence for all cookies, pixels, and tags to verify consent capture and functional opt-out mechanisms.

2. Learn from Marketing to Train Your People. If your compliance training is a dry, text-heavy annual module, people will forget it. Look at what works in marketing: engagement, storytelling, and interactivity. Borrow these tactics. Use diverse media, break information into digestible chapters, and create visual cues to make key policies stick. Effective training builds your human firewall, which is your first and last line of defense.

3. Leverage Templates to Build Consistency. You don't need to start from zero. A wealth of professional templates exists to structure your IT compliance efforts, from incident response plans and disaster recovery playbooks to security policies and change management logs. These tools provide a consistent framework, save immense time, and ensure you're aligning with best practices and major standards from the start.

The goal isn't to stifle innovation but to enable it safely. By putting governance around third parties, engaging your team with better training, and building on proven frameworks, you turn IT compliance from a bottleneck into a business enabler.

Which of these three areas, vendor governance, training, or documentation, is the most pressing gap in your organization right now?

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Let's be clear: in highly regulated industries, information is abundant, but insight is scarce. The critical bridge betw...
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.

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Navigating the New Era of Cosmetics Registration in BangladeshThinking of launching or importing cosmetic products in Ba...
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.

Navigating the Landscape of Regulatory Affairs JobsThe world of regulatory affairs jobs is more dynamic than ever. With ...
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.

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