Manuela Nait
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Manuela Nait Email & Phone Number

Regulatory Affairs Consultant at Pharma D&S
Location: Naples, Campania, Italy 6 work roles 3 schools
1 work email found @alten.it LinkedIn matched
✓ Verified Jul 2026 4 data sources Profile completeness 86%

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Work email m****@alten.it
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Current company
Role
Regulatory Affairs Consultant
Location
Naples, Campania, Italy
Company size

Who is Manuela Nait? Overview

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Quick answer

Manuela Nait is listed as Regulatory Affairs Consultant at Pharma D&S, a with 64 employees, based in Naples, Campania, Italy. AeroLeads shows a work email signal at alten.it and a matched LinkedIn profile for Manuela Nait.

Manuela Nait previously worked as Regulatory Affairs Specialist - Sanofi at Alten Italia and Regulatory Affairs and Site Compliance Specialist - Pfizer at Alten Italia. Manuela Nait holds Master, Regulatory Affairs from M-Squared Consulting.

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{first}.{last}@alten.it
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AeroLeads found 1 current-domain work email signal for Manuela Nait. Compare company email patterns before reaching out.

Profile bio

About Manuela Nait

Laureata in Chimica e Tecnologie Farmaceutiche presso la “Sapienza” Università di Roma. Da sempre appassionata al mondo Pharma, dopo aver svolto una tesi sperimentale in Tecnologia Farmaceutica e aver conseguito l’abilitazione alla professione di Farmacista, ho deciso di ampliare e approfondire le mie conoscenze, intraprendendo un Master in Affari Regolatori.

Current workplace

Manuela Nait's current company

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Pharma D&S
Pharma D&S
Regulatory Affairs Consultant
firenze, tuscany, italy
Website
Employees
64
AeroLeads page
6 roles

Manuela Nait work experience

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Regulatory Affairs Consultant

Current

Napoli

May 2024 - Present

Regulatory Affairs Specialist - Sanofi

Expert in Evaluation and Review of Common Technical Documents (CTD)- Conduct detailed assessments of Common Technical Documents (CTD) related to products marketed in Europe and internationally- Evaluate the compliance of CTD with the latest State-of-the-Art standard and guidelines from international bodies, such as ICH, FDA and European regulatory authorities- Formulate strategic guidance based on the findings from the Gap analysis, to support corporate decision-making, aligning strategies with regulatory compliance and optimal document quality

Dec 2023 - May 2024

Regulatory Affairs And Site Compliance Specialist - Pfizer

Roma

Management of post-marketing regulatory activities of pharmaceutical products marketed in EU and ROW:- Evaluate the regulatory requirements and guidelines applicable to specifc product and region- Preparation and review CTD sections related to Module 3, such as manufacturing process, specification, stability data, batch record and methods- Draw up the CMC documentation for UE and ROW countries regarding license renewals, variations, responses to queries from Health Authorities- Preparation of Regional documents (Declarations, Certificate of Analysis, Application Form for Japan, CPID for Canada, Annual Report for Brazil and US), in order to satisfy the requirement of a specific market- Gap assessment and Compliance review projects

Mar 2022 - Dec 2023

Regulatory Affairs Consultant

Roma

- Collaboration with client companies to suggest the better regulatory strategy and manage the regulatory activities of pharmaceutical products marketed in Italy and EU - Preparation of documents required to the submission of new drug application or a variation at the Health Authority, updating the impacted CTD sections (Module 3) and documents related to the Module 1 (Cover Letter, Application Form, Present and Proposed)- Preparation of eCTD sequence (eCTD manager)- Submission of variantions on AIFA Front End Portal and on the CESP Portal for pharmaceutical products approved with European Procedures-Preparation of articles to published in OJ

Nov 2021 - Mar 2022

Tesi Sperimentale In Tecnologia Farmaceutica

Roma

Tesi sperimentale in Tecnologia Farmaceutica, “Sviluppo e caratterizzazione di Nanohydrogels ad uso oftalmico per la veicolazione di farmaci”. Il lavoro di tesi è stato svolto presso i laboratori del Dipartimento di Chimica e Tecnologia del Farmaco, in collaborazione con l’industria farmaceutica Tubilux Pharma S.P.A., Pomezia (RM).

Sep 2020 - Jun 2021

Studente Tirocinante

Farmacia "Dott. Fortunato"

Sapri, Campania, Italia

Assistenza alle mansioni del farmacista, in particolare dispensazione dei farmaci e utilizzo del software di gestione per la tariffazione delle ricette.

Jul 2019 - Feb 2020
Team & coworkers

Colleagues at Pharma D&S

Other employees you can reach at pharmades.it. View company contacts for 64 employees →

3 education records

Manuela Nait education

Master, Regulatory Affairs

M-Squared Consulting

Diploma, 100

Liceo Scientifico "Carlo Pisacane"
FAQ

Frequently asked questions about Manuela Nait

Quick answers generated from the profile data available on this page.

What company does Manuela Nait work for?

Manuela Nait works for Pharma D&S.

What is Manuela Nait's role at Pharma D&S?

Manuela Nait is listed as Regulatory Affairs Consultant at Pharma D&S.

What is Manuela Nait's email address?

AeroLeads has found 1 work email signal at @alten.it for Manuela Nait at Pharma D&S.

Where is Manuela Nait based?

Manuela Nait is based in Naples, Campania, Italy while working with Pharma D&S.

What companies has Manuela Nait worked for?

Manuela Nait has worked for Pharma D&S, Alten Italia, Di Renzo Regulatory Affairs, Sapienza Università Di Roma, and Farmacia "Dott. Fortunato".

Who are Manuela Nait's colleagues at Pharma D&S?

Manuela Nait's colleagues at Pharma D&S include Aurelio Natta, Giovanna Gregori, Cristiana Bramanti, Giuliana Amato, and Gianni Montaini, Phd.

How can I contact Manuela Nait?

You can use AeroLeads to view verified contact signals for Manuela Nait at Pharma D&S, including work email, phone, and LinkedIn data when available.

What schools did Manuela Nait attend?

Manuela Nait holds Master, Regulatory Affairs from M-Squared Consulting.

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